Canonical Allele Identifier: CA1321140583

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640238A= , CM000664.2:g.201640238A=	GRCh38
NC_000002.11:g.202504961A= , CM000664.1:g.202504961A=	GRCh37
NC_000002.10:g.202213206A=	NCBI36
NG_032049.1:g.8292T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.-356+655T=	ENSP00000480508.2:n.-356+655T=
ENST00000409883.7:c.79+23T= MANE Select	ENSP00000386264.2:n.79+23T=
ENST00000286196.9:c.-1+655T=	ENSP00000286196.5:n.-1+655T=
ENST00000409444.6:c.55+23T=	ENSP00000387203.2:n.55+23T=
ENST00000409883.6:c.79+23T=	ENSP00000386264.2:n.79+23T=
ENST00000432684.6:c.79+23T=	ENSP00000413230.2:n.79+23T=
ENST00000444047.6:c.79+23T=	ENSP00000402681.2:n.79+23T=
ENST00000463205.2:n.82+23T=
ENST00000489550.5:n.92+655T=
ENST00000621467.4:c.50+655T=	ENSP00000480508.1:n.50+655T=
NM_001044385.2:c.79+23T=	NP_001037850.1:n.79+23T=
NM_152388.3:c.55+23T=	NP_689601.2:n.55+23T=
NM_001044385.3:c.79+23T= MANE Select	NP_001037850.1:n.79+23T=
NM_152388.4:c.55+23T=	NP_689601.2:n.55+23T=