Canonical Allele Identifier: CA350304478

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490803C>A (hg19) ; chr2:g.201626080C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626080C>A , CM000664.2:g.201626080C>A	GRCh38
NC_000002.11:g.202490803C>A , CM000664.1:g.202490803C>A	GRCh37
NC_000002.10:g.202199048C>A	NCBI36
NG_032049.1:g.22450G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.901G>T
ENST00000621467.5:c.979G>T	ENSP00000480508.2:p.Val327Phe
ENST00000686475.1:n.1045G>T
ENST00000409883.7:c.1105G>T MANE Select	ENSP00000386264.2:p.Val369Phe
ENST00000286196.9:c.*669G>T	ENSP00000286196.5:n.*669G>T
ENST00000409444.6:c.1081G>T	ENSP00000387203.2:p.Val361Phe
ENST00000409883.6:c.1105G>T	ENSP00000386264.2:p.Val369Phe
ENST00000471318.5:n.333G>T
ENST00000495329.1:n.244G>T
ENST00000621467.4:c.1081G>T	ENSP00000480508.1:p.Val361Phe
NM_001044385.2:c.1105G>T	NP_001037850.1:p.Val369Phe
NM_152388.3:c.1081G>T	NP_689601.2:p.Val361Phe
NM_001044385.3:c.1105G>T MANE Select	NP_001037850.1:p.Val369Phe
NM_152388.4:c.1081G>T	NP_689601.2:p.Val361Phe