Canonical Allele Identifier: CA1572383529
Gene: TMEM232 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110672536_110672549delinsGAAAAAATAGCCAA , CM000667.2:g.110672536_110672549delinsGAAAAAATAGCCAA GRCh38
NC_000005.9:g.110008237_110008250delinsGAAAAAATAGCCAA , CM000667.1:g.110008237_110008250delinsGAAAAAATAGCCAA GRCh37
NC_000005.8:g.110036136_110036149delinsGAAAAAATAGCCAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455884.7:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC MANE Select ENSP00000401477.2:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
ENST00000455884.6:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC ENSP00000401477.2:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
ENST00000502857.6:n.80-5185_80-5172delinsTTGGCTATTTTTTC
ENST00000503527.6:n.311-5185_311-5172delinsTTGGCTATTTTTTC
ENST00000511883.6:c.-47-4820_-47-4807delinsTTGGCTATTTTTTC ENSP00000423904.2:n.-47-4820_-47-4807delinsTTGGCTATTTTTTC
ENST00000512003.7:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC ENSP00000427785.2:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
ENST00000512577.5:n.397-5185_397-5172delinsTTGGCTATTTTTTC
ENST00000512886.5:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC ENSP00000424807.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
ENST00000515278.6:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC ENSP00000421614.2:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
ENST00000515518.6:n.46-30178_46-30165delinsTTGGCTATTTTTTC
NM_001039763.3:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC NP_001034852.3:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_006714670.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_006714733.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543552.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541854.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543554.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541856.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543555.1:c.69-30178_69-30165delinsTTGGCTATTTTTTC XP_011541857.1:n.69-30178_69-30165delinsTTGGCTATTTTTTC
XM_011543556.1:c.69-30178_69-30165delinsTTGGCTATTTTTTC XP_011541858.1:n.69-30178_69-30165delinsTTGGCTATTTTTTC
XM_011543557.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541859.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543558.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541860.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543559.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541861.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543561.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541863.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543562.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541864.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543563.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541865.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543564.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541866.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543565.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541867.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543566.1:c.-215-30178_-215-30165delinsTTGGCTATTTTTTC XP_011541868.1:n.-215-30178_-215-30165delinsTTGGCTATTTTTTC
XM_011543567.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541869.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543568.1:c.-229-30178_-229-30165delinsTTGGCTATTTTTTC XP_011541870.1:n.-229-30178_-229-30165delinsTTGGCTATTTTTTC
XR_948284.1:n.837-5185_837-5172delinsTTGGCTATTTTTTC
XR_948285.1:n.837-5185_837-5172delinsTTGGCTATTTTTTC
XR_948286.1:n.837-5185_837-5172delinsTTGGCTATTTTTTC
XR_948287.1:n.836-5185_836-5172delinsTTGGCTATTTTTTC
XM_006714670.3:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_006714733.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543552.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541854.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543555.2:c.69-30178_69-30165delinsTTGGCTATTTTTTC XP_011541857.1:n.69-30178_69-30165delinsTTGGCTATTTTTTC
XM_011543556.2:c.69-30178_69-30165delinsTTGGCTATTTTTTC XP_011541858.1:n.69-30178_69-30165delinsTTGGCTATTTTTTC
XM_011543557.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541859.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543559.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541861.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543561.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541863.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543563.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541865.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543564.3:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541866.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543565.3:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541867.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_011543566.2:c.-215-30178_-215-30165delinsTTGGCTATTTTTTC XP_011541868.1:n.-215-30178_-215-30165delinsTTGGCTATTTTTTC
XM_011543567.3:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_011541869.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_017009705.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_016865194.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_017009706.2:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_016865195.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XM_017009707.1:c.-352-5185_-352-5172delinsTTGGCTATTTTTTC XP_016865196.1:n.-352-5185_-352-5172delinsTTGGCTATTTTTTC
XM_024446149.1:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC XP_024301917.1:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC
XR_001742181.1:n.851-5185_851-5172delinsTTGGCTATTTTTTC
XR_001742182.1:n.850-5185_850-5172delinsTTGGCTATTTTTTC
XR_948284.2:n.852-5185_852-5172delinsTTGGCTATTTTTTC
XR_948285.2:n.851-5185_851-5172delinsTTGGCTATTTTTTC
XR_948287.2:n.850-5185_850-5172delinsTTGGCTATTTTTTC
NM_001039763.4:c.-12-5185_-12-5172delinsTTGGCTATTTTTTC MANE Select NP_001034852.3:n.-12-5185_-12-5172delinsTTGGCTATTTTTTC