Canonical Allele Identifier: CA1321143702

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623470G= , CM000664.2:g.201623470G=	GRCh38
NC_000002.11:g.202488193G= , CM000664.1:g.202488193G=	GRCh37
NC_000002.10:g.202196438G=	NCBI36
NG_032049.1:g.25060C=
NG_051007.1:g.713C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*785C=	ENSP00000480508.2:n.*785C=
ENST00000686475.1:n.1952C=
ENST00000409883.7:c.*785C= MANE Select	ENSP00000386264.2:n.*785C=
ENST00000409444.6:c.*785C=	ENSP00000387203.2:n.*785C=
ENST00000409883.6:c.*785C=	ENSP00000386264.2:n.*785C=
ENST00000495329.1:n.1151C=
NM_001044385.2:c.*785C=	NP_001037850.1:n.*785C=
NM_152388.3:c.*785C=	NP_689601.2:n.*785C=
NM_001044385.3:c.*785C= MANE Select	NP_001037850.1:n.*785C=
NM_152388.4:c.*785C=	NP_689601.2:n.*785C=