Canonical Allele Identifier: CA1321145735

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625942_201625943delinsTA , CM000664.2:g.201625942_201625943delinsTA	GRCh38
NC_000002.11:g.202490665_202490666delinsTA , CM000664.1:g.202490665_202490666delinsTA	GRCh37
NC_000002.10:g.202198910_202198911delinsTA	NCBI36
NG_032049.1:g.22587_22588delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+83_955+84delinsTA
ENST00000621467.5:c.1033+83_1033+84delinsTA	ENSP00000480508.2:n.1033+83_1033+84delinsTA
ENST00000686475.1:n.1099+83_1099+84delinsTA
ENST00000409883.7:c.1159+83_1159+84delinsTA MANE Select	ENSP00000386264.2:n.1159+83_1159+84delinsTA
ENST00000286196.9:c.*723+83_*723+84delinsTA	ENSP00000286196.5:n.*723+83_*723+84delinsTA
ENST00000409444.6:c.1135+83_1135+84delinsTA	ENSP00000387203.2:n.1135+83_1135+84delinsTA
ENST00000409883.6:c.1159+83_1159+84delinsTA	ENSP00000386264.2:n.1159+83_1159+84delinsTA
ENST00000471318.5:n.387+83_387+84delinsTA
ENST00000495329.1:n.298+83_298+84delinsTA
ENST00000621467.4:c.1135+83_1135+84delinsTA	ENSP00000480508.1:n.1135+83_1135+84delinsTA
NM_001044385.2:c.1159+83_1159+84delinsTA	NP_001037850.1:n.1159+83_1159+84delinsTA
NM_152388.3:c.1135+83_1135+84delinsTA	NP_689601.2:n.1135+83_1135+84delinsTA
NM_001044385.3:c.1159+83_1159+84delinsTA MANE Select	NP_001037850.1:n.1159+83_1159+84delinsTA
NM_152388.4:c.1135+83_1135+84delinsTA	NP_689601.2:n.1135+83_1135+84delinsTA