Canonical Allele Identifier: CA1572383587
Gene: TMEM232 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110672577_110672578delinsGA , CM000667.2:g.110672577_110672578delinsGA GRCh38
NC_000005.9:g.110008278_110008279delinsGA , CM000667.1:g.110008278_110008279delinsGA GRCh37
NC_000005.8:g.110036177_110036178delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455884.7:c.-12-5214_-12-5213delinsTC MANE Select ENSP00000401477.2:n.-12-5214_-12-5213delinsTC
ENST00000455884.6:c.-12-5214_-12-5213delinsTC ENSP00000401477.2:n.-12-5214_-12-5213delinsTC
ENST00000502857.6:n.80-5214_80-5213delinsTC
ENST00000503527.6:n.311-5214_311-5213delinsTC
ENST00000511883.6:c.-47-4849_-47-4848delinsTC ENSP00000423904.2:n.-47-4849_-47-4848delinsTC
ENST00000512003.7:c.-12-5214_-12-5213delinsTC ENSP00000427785.2:n.-12-5214_-12-5213delinsTC
ENST00000512577.5:n.397-5214_397-5213delinsTC
ENST00000512886.5:c.-12-5214_-12-5213delinsTC ENSP00000424807.1:n.-12-5214_-12-5213delinsTC
ENST00000515278.6:c.-12-5214_-12-5213delinsTC ENSP00000421614.2:n.-12-5214_-12-5213delinsTC
ENST00000515518.6:n.46-30207_46-30206delinsTC
NM_001039763.3:c.-12-5214_-12-5213delinsTC NP_001034852.3:n.-12-5214_-12-5213delinsTC
XM_006714670.2:c.-12-5214_-12-5213delinsTC XP_006714733.1:n.-12-5214_-12-5213delinsTC
XM_011543552.1:c.-12-5214_-12-5213delinsTC XP_011541854.1:n.-12-5214_-12-5213delinsTC
XM_011543554.1:c.-12-5214_-12-5213delinsTC XP_011541856.1:n.-12-5214_-12-5213delinsTC
XM_011543555.1:c.69-30207_69-30206delinsTC XP_011541857.1:n.69-30207_69-30206delinsTC
XM_011543556.1:c.69-30207_69-30206delinsTC XP_011541858.1:n.69-30207_69-30206delinsTC
XM_011543557.1:c.-12-5214_-12-5213delinsTC XP_011541859.1:n.-12-5214_-12-5213delinsTC
XM_011543558.1:c.-12-5214_-12-5213delinsTC XP_011541860.1:n.-12-5214_-12-5213delinsTC
XM_011543559.1:c.-12-5214_-12-5213delinsTC XP_011541861.1:n.-12-5214_-12-5213delinsTC
XM_011543561.1:c.-12-5214_-12-5213delinsTC XP_011541863.1:n.-12-5214_-12-5213delinsTC
XM_011543562.1:c.-12-5214_-12-5213delinsTC XP_011541864.1:n.-12-5214_-12-5213delinsTC
XM_011543563.1:c.-12-5214_-12-5213delinsTC XP_011541865.1:n.-12-5214_-12-5213delinsTC
XM_011543564.1:c.-12-5214_-12-5213delinsTC XP_011541866.1:n.-12-5214_-12-5213delinsTC
XM_011543565.1:c.-12-5214_-12-5213delinsTC XP_011541867.1:n.-12-5214_-12-5213delinsTC
XM_011543566.1:c.-215-30207_-215-30206delinsTC XP_011541868.1:n.-215-30207_-215-30206delinsTC
XM_011543567.1:c.-12-5214_-12-5213delinsTC XP_011541869.1:n.-12-5214_-12-5213delinsTC
XM_011543568.1:c.-229-30207_-229-30206delinsTC XP_011541870.1:n.-229-30207_-229-30206delinsTC
XR_948284.1:n.837-5214_837-5213delinsTC
XR_948285.1:n.837-5214_837-5213delinsTC
XR_948286.1:n.837-5214_837-5213delinsTC
XR_948287.1:n.836-5214_836-5213delinsTC
XM_006714670.3:c.-12-5214_-12-5213delinsTC XP_006714733.1:n.-12-5214_-12-5213delinsTC
XM_011543552.2:c.-12-5214_-12-5213delinsTC XP_011541854.1:n.-12-5214_-12-5213delinsTC
XM_011543555.2:c.69-30207_69-30206delinsTC XP_011541857.1:n.69-30207_69-30206delinsTC
XM_011543556.2:c.69-30207_69-30206delinsTC XP_011541858.1:n.69-30207_69-30206delinsTC
XM_011543557.2:c.-12-5214_-12-5213delinsTC XP_011541859.1:n.-12-5214_-12-5213delinsTC
XM_011543559.2:c.-12-5214_-12-5213delinsTC XP_011541861.1:n.-12-5214_-12-5213delinsTC
XM_011543561.2:c.-12-5214_-12-5213delinsTC XP_011541863.1:n.-12-5214_-12-5213delinsTC
XM_011543563.2:c.-12-5214_-12-5213delinsTC XP_011541865.1:n.-12-5214_-12-5213delinsTC
XM_011543564.3:c.-12-5214_-12-5213delinsTC XP_011541866.1:n.-12-5214_-12-5213delinsTC
XM_011543565.3:c.-12-5214_-12-5213delinsTC XP_011541867.1:n.-12-5214_-12-5213delinsTC
XM_011543566.2:c.-215-30207_-215-30206delinsTC XP_011541868.1:n.-215-30207_-215-30206delinsTC
XM_011543567.3:c.-12-5214_-12-5213delinsTC XP_011541869.1:n.-12-5214_-12-5213delinsTC
XM_017009705.2:c.-12-5214_-12-5213delinsTC XP_016865194.1:n.-12-5214_-12-5213delinsTC
XM_017009706.2:c.-12-5214_-12-5213delinsTC XP_016865195.1:n.-12-5214_-12-5213delinsTC
XM_017009707.1:c.-352-5214_-352-5213delinsTC XP_016865196.1:n.-352-5214_-352-5213delinsTC
XM_024446149.1:c.-12-5214_-12-5213delinsTC XP_024301917.1:n.-12-5214_-12-5213delinsTC
XR_001742181.1:n.851-5214_851-5213delinsTC
XR_001742182.1:n.850-5214_850-5213delinsTC
XR_948284.2:n.852-5214_852-5213delinsTC
XR_948285.2:n.851-5214_851-5213delinsTC
XR_948287.2:n.850-5214_850-5213delinsTC
NM_001039763.4:c.-12-5214_-12-5213delinsTC MANE Select NP_001034852.3:n.-12-5214_-12-5213delinsTC