Canonical Allele Identifier: CA350304769

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490850T>A (hg19) ; chr2:g.201626127T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626127T>A , CM000664.2:g.201626127T>A	GRCh38
NC_000002.11:g.202490850T>A , CM000664.1:g.202490850T>A	GRCh37
NC_000002.10:g.202199095T>A	NCBI36
NG_032049.1:g.22403A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.854A>T
ENST00000621467.5:c.932A>T	ENSP00000480508.2:p.Gln311Leu
ENST00000686475.1:n.998A>T
ENST00000409883.7:c.1058A>T MANE Select	ENSP00000386264.2:p.Gln353Leu
ENST00000286196.9:c.*622A>T	ENSP00000286196.5:n.*622A>T
ENST00000409444.6:c.1034A>T	ENSP00000387203.2:p.Gln345Leu
ENST00000409883.6:c.1058A>T	ENSP00000386264.2:p.Gln353Leu
ENST00000471318.5:n.286A>T
ENST00000495329.1:n.197A>T
ENST00000621467.4:c.1034A>T	ENSP00000480508.1:p.Gln345Leu
NM_001044385.2:c.1058A>T	NP_001037850.1:p.Gln353Leu
NM_152388.3:c.1034A>T	NP_689601.2:p.Gln345Leu
NM_001044385.3:c.1058A>T MANE Select	NP_001037850.1:p.Gln353Leu
NM_152388.4:c.1034A>T	NP_689601.2:p.Gln345Leu