Canonical Allele Identifier: CA350304524

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490814A>G (hg19) ; chr2:g.201626091A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626091A>G , CM000664.2:g.201626091A>G	GRCh38
NC_000002.11:g.202490814A>G , CM000664.1:g.202490814A>G	GRCh37
NC_000002.10:g.202199059A>G	NCBI36
NG_032049.1:g.22439T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.890T>C
ENST00000621467.5:c.968T>C	ENSP00000480508.2:p.Val323Ala
ENST00000686475.1:n.1034T>C
ENST00000409883.7:c.1094T>C MANE Select	ENSP00000386264.2:p.Val365Ala
ENST00000286196.9:c.*658T>C	ENSP00000286196.5:n.*658T>C
ENST00000409444.6:c.1070T>C	ENSP00000387203.2:p.Val357Ala
ENST00000409883.6:c.1094T>C	ENSP00000386264.2:p.Val365Ala
ENST00000471318.5:n.322T>C
ENST00000495329.1:n.233T>C
ENST00000621467.4:c.1070T>C	ENSP00000480508.1:p.Val357Ala
NM_001044385.2:c.1094T>C	NP_001037850.1:p.Val365Ala
NM_152388.3:c.1070T>C	NP_689601.2:p.Val357Ala
NM_001044385.3:c.1094T>C MANE Select	NP_001037850.1:p.Val365Ala
NM_152388.4:c.1070T>C	NP_689601.2:p.Val357Ala