Canonical Allele Identifier: CA1321143679

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623447T= , CM000664.2:g.201623447T=	GRCh38
NC_000002.11:g.202488170T= , CM000664.1:g.202488170T=	GRCh37
NC_000002.10:g.202196415T=	NCBI36
NG_032049.1:g.25083A=
NG_051007.1:g.736A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*808A=	ENSP00000480508.2:n.*808A=
ENST00000686475.1:n.1975A=
ENST00000409883.7:c.*808A= MANE Select	ENSP00000386264.2:n.*808A=
ENST00000409444.6:c.*808A=	ENSP00000387203.2:n.*808A=
ENST00000409883.6:c.*808A=	ENSP00000386264.2:n.*808A=
ENST00000495329.1:n.1174A=
NM_001044385.2:c.*808A=	NP_001037850.1:n.*808A=
NM_152388.3:c.*808A=	NP_689601.2:n.*808A=
NM_001044385.3:c.*808A= MANE Select	NP_001037850.1:n.*808A=
NM_152388.4:c.*808A=	NP_689601.2:n.*808A=