Canonical Allele Identifier: CA1321145539

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625695A= , CM000664.2:g.201625695A=	GRCh38
NC_000002.11:g.202490418A= , CM000664.1:g.202490418A=	GRCh37
NC_000002.10:g.202198663A=	NCBI36
NG_032049.1:g.22835T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+331T=
ENST00000621467.5:c.1033+331T=	ENSP00000480508.2:n.1033+331T=
ENST00000686475.1:n.1099+331T=
ENST00000409883.7:c.1159+331T= MANE Select	ENSP00000386264.2:n.1159+331T=
ENST00000286196.9:c.*723+331T=	ENSP00000286196.5:n.*723+331T=
ENST00000409444.6:c.1135+331T=	ENSP00000387203.2:n.1135+331T=
ENST00000409883.6:c.1159+331T=	ENSP00000386264.2:n.1159+331T=
ENST00000471318.5:n.387+331T=
ENST00000495329.1:n.298+331T=
ENST00000621467.4:c.1135+331T=	ENSP00000480508.1:n.1135+331T=
NM_001044385.2:c.1159+331T=	NP_001037850.1:n.1159+331T=
NM_152388.3:c.1135+331T=	NP_689601.2:n.1135+331T=
NM_001044385.3:c.1159+331T= MANE Select	NP_001037850.1:n.1159+331T=
NM_152388.4:c.1135+331T=	NP_689601.2:n.1135+331T=