Canonical Allele Identifier: CA1321145794

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626008_201626009delinsAT , CM000664.2:g.201626008_201626009delinsAT	GRCh38
NC_000002.11:g.202490731_202490732delinsAT , CM000664.1:g.202490731_202490732delinsAT	GRCh37
NC_000002.10:g.202198976_202198977delinsAT	NCBI36
NG_032049.1:g.22521_22522delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+17_955+18delinsAT
ENST00000621467.5:c.1033+17_1033+18delinsAT	ENSP00000480508.2:n.1033+17_1033+18delinsAT
ENST00000686475.1:n.1099+17_1099+18delinsAT
ENST00000409883.7:c.1159+17_1159+18delinsAT MANE Select	ENSP00000386264.2:n.1159+17_1159+18delinsAT
ENST00000286196.9:c.*723+17_*723+18delinsAT	ENSP00000286196.5:n.*723+17_*723+18delinsAT
ENST00000409444.6:c.1135+17_1135+18delinsAT	ENSP00000387203.2:n.1135+17_1135+18delinsAT
ENST00000409883.6:c.1159+17_1159+18delinsAT	ENSP00000386264.2:n.1159+17_1159+18delinsAT
ENST00000471318.5:n.387+17_387+18delinsAT
ENST00000495329.1:n.298+17_298+18delinsAT
ENST00000621467.4:c.1135+17_1135+18delinsAT	ENSP00000480508.1:n.1135+17_1135+18delinsAT
NM_001044385.2:c.1159+17_1159+18delinsAT	NP_001037850.1:n.1159+17_1159+18delinsAT
NM_152388.3:c.1135+17_1135+18delinsAT	NP_689601.2:n.1135+17_1135+18delinsAT
NM_001044385.3:c.1159+17_1159+18delinsAT MANE Select	NP_001037850.1:n.1159+17_1159+18delinsAT
NM_152388.4:c.1135+17_1135+18delinsAT	NP_689601.2:n.1135+17_1135+18delinsAT