Canonical Allele Identifier: CA1572383547

Gene: TMEM232

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110672557_110672558delinsCA , CM000667.2:g.110672557_110672558delinsCA	GRCh38
NC_000005.9:g.110008258_110008259delinsCA , CM000667.1:g.110008258_110008259delinsCA	GRCh37
NC_000005.8:g.110036157_110036158delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455884.7:c.-12-5194_-12-5193delinsTG MANE Select	ENSP00000401477.2:n.-12-5194_-12-5193delinsTG
ENST00000455884.6:c.-12-5194_-12-5193delinsTG	ENSP00000401477.2:n.-12-5194_-12-5193delinsTG
ENST00000502857.6:n.80-5194_80-5193delinsTG
ENST00000503527.6:n.311-5194_311-5193delinsTG
ENST00000511883.6:c.-47-4829_-47-4828delinsTG	ENSP00000423904.2:n.-47-4829_-47-4828delinsTG
ENST00000512003.7:c.-12-5194_-12-5193delinsTG	ENSP00000427785.2:n.-12-5194_-12-5193delinsTG
ENST00000512577.5:n.397-5194_397-5193delinsTG
ENST00000512886.5:c.-12-5194_-12-5193delinsTG	ENSP00000424807.1:n.-12-5194_-12-5193delinsTG
ENST00000515278.6:c.-12-5194_-12-5193delinsTG	ENSP00000421614.2:n.-12-5194_-12-5193delinsTG
ENST00000515518.6:n.46-30187_46-30186delinsTG
NM_001039763.3:c.-12-5194_-12-5193delinsTG	NP_001034852.3:n.-12-5194_-12-5193delinsTG
XM_006714670.2:c.-12-5194_-12-5193delinsTG	XP_006714733.1:n.-12-5194_-12-5193delinsTG
XM_011543552.1:c.-12-5194_-12-5193delinsTG	XP_011541854.1:n.-12-5194_-12-5193delinsTG
XM_011543554.1:c.-12-5194_-12-5193delinsTG	XP_011541856.1:n.-12-5194_-12-5193delinsTG
XM_011543555.1:c.69-30187_69-30186delinsTG	XP_011541857.1:n.69-30187_69-30186delinsTG
XM_011543556.1:c.69-30187_69-30186delinsTG	XP_011541858.1:n.69-30187_69-30186delinsTG
XM_011543557.1:c.-12-5194_-12-5193delinsTG	XP_011541859.1:n.-12-5194_-12-5193delinsTG
XM_011543558.1:c.-12-5194_-12-5193delinsTG	XP_011541860.1:n.-12-5194_-12-5193delinsTG
XM_011543559.1:c.-12-5194_-12-5193delinsTG	XP_011541861.1:n.-12-5194_-12-5193delinsTG
XM_011543561.1:c.-12-5194_-12-5193delinsTG	XP_011541863.1:n.-12-5194_-12-5193delinsTG
XM_011543562.1:c.-12-5194_-12-5193delinsTG	XP_011541864.1:n.-12-5194_-12-5193delinsTG
XM_011543563.1:c.-12-5194_-12-5193delinsTG	XP_011541865.1:n.-12-5194_-12-5193delinsTG
XM_011543564.1:c.-12-5194_-12-5193delinsTG	XP_011541866.1:n.-12-5194_-12-5193delinsTG
XM_011543565.1:c.-12-5194_-12-5193delinsTG	XP_011541867.1:n.-12-5194_-12-5193delinsTG
XM_011543566.1:c.-215-30187_-215-30186delinsTG	XP_011541868.1:n.-215-30187_-215-30186delinsTG
XM_011543567.1:c.-12-5194_-12-5193delinsTG	XP_011541869.1:n.-12-5194_-12-5193delinsTG
XM_011543568.1:c.-229-30187_-229-30186delinsTG	XP_011541870.1:n.-229-30187_-229-30186delinsTG
XR_948284.1:n.837-5194_837-5193delinsTG
XR_948285.1:n.837-5194_837-5193delinsTG
XR_948286.1:n.837-5194_837-5193delinsTG
XR_948287.1:n.836-5194_836-5193delinsTG
XM_006714670.3:c.-12-5194_-12-5193delinsTG	XP_006714733.1:n.-12-5194_-12-5193delinsTG
XM_011543552.2:c.-12-5194_-12-5193delinsTG	XP_011541854.1:n.-12-5194_-12-5193delinsTG
XM_011543555.2:c.69-30187_69-30186delinsTG	XP_011541857.1:n.69-30187_69-30186delinsTG
XM_011543556.2:c.69-30187_69-30186delinsTG	XP_011541858.1:n.69-30187_69-30186delinsTG
XM_011543557.2:c.-12-5194_-12-5193delinsTG	XP_011541859.1:n.-12-5194_-12-5193delinsTG
XM_011543559.2:c.-12-5194_-12-5193delinsTG	XP_011541861.1:n.-12-5194_-12-5193delinsTG
XM_011543561.2:c.-12-5194_-12-5193delinsTG	XP_011541863.1:n.-12-5194_-12-5193delinsTG
XM_011543563.2:c.-12-5194_-12-5193delinsTG	XP_011541865.1:n.-12-5194_-12-5193delinsTG
XM_011543564.3:c.-12-5194_-12-5193delinsTG	XP_011541866.1:n.-12-5194_-12-5193delinsTG
XM_011543565.3:c.-12-5194_-12-5193delinsTG	XP_011541867.1:n.-12-5194_-12-5193delinsTG
XM_011543566.2:c.-215-30187_-215-30186delinsTG	XP_011541868.1:n.-215-30187_-215-30186delinsTG
XM_011543567.3:c.-12-5194_-12-5193delinsTG	XP_011541869.1:n.-12-5194_-12-5193delinsTG
XM_017009705.2:c.-12-5194_-12-5193delinsTG	XP_016865194.1:n.-12-5194_-12-5193delinsTG
XM_017009706.2:c.-12-5194_-12-5193delinsTG	XP_016865195.1:n.-12-5194_-12-5193delinsTG
XM_017009707.1:c.-352-5194_-352-5193delinsTG	XP_016865196.1:n.-352-5194_-352-5193delinsTG
XM_024446149.1:c.-12-5194_-12-5193delinsTG	XP_024301917.1:n.-12-5194_-12-5193delinsTG
XR_001742181.1:n.851-5194_851-5193delinsTG
XR_001742182.1:n.850-5194_850-5193delinsTG
XR_948284.2:n.852-5194_852-5193delinsTG
XR_948285.2:n.851-5194_851-5193delinsTG
XR_948287.2:n.850-5194_850-5193delinsTG
NM_001039763.4:c.-12-5194_-12-5193delinsTG MANE Select	NP_001034852.3:n.-12-5194_-12-5193delinsTG