Canonical Allele Identifier: CA1572383614
Gene: TMEM232 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110672594_110672595delinsTA , CM000667.2:g.110672594_110672595delinsTA GRCh38
NC_000005.9:g.110008295_110008296delinsTA , CM000667.1:g.110008295_110008296delinsTA GRCh37
NC_000005.8:g.110036194_110036195delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455884.7:c.-12-5231_-12-5230delinsTA MANE Select ENSP00000401477.2:n.-12-5231_-12-5230delinsTA
ENST00000455884.6:c.-12-5231_-12-5230delinsTA ENSP00000401477.2:n.-12-5231_-12-5230delinsTA
ENST00000502857.6:n.80-5231_80-5230delinsTA
ENST00000503527.6:n.311-5231_311-5230delinsTA
ENST00000511883.6:c.-47-4866_-47-4865delinsTA ENSP00000423904.2:n.-47-4866_-47-4865delinsTA
ENST00000512003.7:c.-12-5231_-12-5230delinsTA ENSP00000427785.2:n.-12-5231_-12-5230delinsTA
ENST00000512577.5:n.397-5231_397-5230delinsTA
ENST00000512886.5:c.-12-5231_-12-5230delinsTA ENSP00000424807.1:n.-12-5231_-12-5230delinsTA
ENST00000515278.6:c.-12-5231_-12-5230delinsTA ENSP00000421614.2:n.-12-5231_-12-5230delinsTA
ENST00000515518.6:n.46-30224_46-30223delinsTA
NM_001039763.3:c.-12-5231_-12-5230delinsTA NP_001034852.3:n.-12-5231_-12-5230delinsTA
XM_006714670.2:c.-12-5231_-12-5230delinsTA XP_006714733.1:n.-12-5231_-12-5230delinsTA
XM_011543552.1:c.-12-5231_-12-5230delinsTA XP_011541854.1:n.-12-5231_-12-5230delinsTA
XM_011543554.1:c.-12-5231_-12-5230delinsTA XP_011541856.1:n.-12-5231_-12-5230delinsTA
XM_011543555.1:c.69-30224_69-30223delinsTA XP_011541857.1:n.69-30224_69-30223delinsTA
XM_011543556.1:c.69-30224_69-30223delinsTA XP_011541858.1:n.69-30224_69-30223delinsTA
XM_011543557.1:c.-12-5231_-12-5230delinsTA XP_011541859.1:n.-12-5231_-12-5230delinsTA
XM_011543558.1:c.-12-5231_-12-5230delinsTA XP_011541860.1:n.-12-5231_-12-5230delinsTA
XM_011543559.1:c.-12-5231_-12-5230delinsTA XP_011541861.1:n.-12-5231_-12-5230delinsTA
XM_011543561.1:c.-12-5231_-12-5230delinsTA XP_011541863.1:n.-12-5231_-12-5230delinsTA
XM_011543562.1:c.-12-5231_-12-5230delinsTA XP_011541864.1:n.-12-5231_-12-5230delinsTA
XM_011543563.1:c.-12-5231_-12-5230delinsTA XP_011541865.1:n.-12-5231_-12-5230delinsTA
XM_011543564.1:c.-12-5231_-12-5230delinsTA XP_011541866.1:n.-12-5231_-12-5230delinsTA
XM_011543565.1:c.-12-5231_-12-5230delinsTA XP_011541867.1:n.-12-5231_-12-5230delinsTA
XM_011543566.1:c.-215-30224_-215-30223delinsTA XP_011541868.1:n.-215-30224_-215-30223delinsTA
XM_011543567.1:c.-12-5231_-12-5230delinsTA XP_011541869.1:n.-12-5231_-12-5230delinsTA
XM_011543568.1:c.-229-30224_-229-30223delinsTA XP_011541870.1:n.-229-30224_-229-30223delinsTA
XR_948284.1:n.837-5231_837-5230delinsTA
XR_948285.1:n.837-5231_837-5230delinsTA
XR_948286.1:n.837-5231_837-5230delinsTA
XR_948287.1:n.836-5231_836-5230delinsTA
XM_006714670.3:c.-12-5231_-12-5230delinsTA XP_006714733.1:n.-12-5231_-12-5230delinsTA
XM_011543552.2:c.-12-5231_-12-5230delinsTA XP_011541854.1:n.-12-5231_-12-5230delinsTA
XM_011543555.2:c.69-30224_69-30223delinsTA XP_011541857.1:n.69-30224_69-30223delinsTA
XM_011543556.2:c.69-30224_69-30223delinsTA XP_011541858.1:n.69-30224_69-30223delinsTA
XM_011543557.2:c.-12-5231_-12-5230delinsTA XP_011541859.1:n.-12-5231_-12-5230delinsTA
XM_011543559.2:c.-12-5231_-12-5230delinsTA XP_011541861.1:n.-12-5231_-12-5230delinsTA
XM_011543561.2:c.-12-5231_-12-5230delinsTA XP_011541863.1:n.-12-5231_-12-5230delinsTA
XM_011543563.2:c.-12-5231_-12-5230delinsTA XP_011541865.1:n.-12-5231_-12-5230delinsTA
XM_011543564.3:c.-12-5231_-12-5230delinsTA XP_011541866.1:n.-12-5231_-12-5230delinsTA
XM_011543565.3:c.-12-5231_-12-5230delinsTA XP_011541867.1:n.-12-5231_-12-5230delinsTA
XM_011543566.2:c.-215-30224_-215-30223delinsTA XP_011541868.1:n.-215-30224_-215-30223delinsTA
XM_011543567.3:c.-12-5231_-12-5230delinsTA XP_011541869.1:n.-12-5231_-12-5230delinsTA
XM_017009705.2:c.-12-5231_-12-5230delinsTA XP_016865194.1:n.-12-5231_-12-5230delinsTA
XM_017009706.2:c.-12-5231_-12-5230delinsTA XP_016865195.1:n.-12-5231_-12-5230delinsTA
XM_017009707.1:c.-352-5231_-352-5230delinsTA XP_016865196.1:n.-352-5231_-352-5230delinsTA
XM_024446149.1:c.-12-5231_-12-5230delinsTA XP_024301917.1:n.-12-5231_-12-5230delinsTA
XR_001742181.1:n.851-5231_851-5230delinsTA
XR_001742182.1:n.850-5231_850-5230delinsTA
XR_948284.2:n.852-5231_852-5230delinsTA
XR_948285.2:n.851-5231_851-5230delinsTA
XR_948287.2:n.850-5231_850-5230delinsTA
NM_001039763.4:c.-12-5231_-12-5230delinsTA MANE Select NP_001034852.3:n.-12-5231_-12-5230delinsTA