Canonical Allele Identifier: CA1321146149

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626252G= , CM000664.2:g.201626252G=	GRCh38
NC_000002.11:g.202490975G= , CM000664.1:g.202490975G=	GRCh37
NC_000002.10:g.202199220G=	NCBI36
NG_032049.1:g.22278C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-105C=
ENST00000621467.5:c.912-105C=	ENSP00000480508.2:n.912-105C=
ENST00000686475.1:n.978-105C=
ENST00000409883.7:c.1038-105C= MANE Select	ENSP00000386264.2:n.1038-105C=
ENST00000286196.9:c.*602-105C=	ENSP00000286196.5:n.*602-105C=
ENST00000409444.6:c.1014-105C=	ENSP00000387203.2:n.1014-105C=
ENST00000409883.6:c.1038-105C=	ENSP00000386264.2:n.1038-105C=
ENST00000471318.5:n.266-105C=
ENST00000495329.1:n.72C=
ENST00000621467.4:c.1014-105C=	ENSP00000480508.1:n.1014-105C=
NM_001044385.2:c.1038-105C=	NP_001037850.1:n.1038-105C=
NM_152388.3:c.1014-105C=	NP_689601.2:n.1014-105C=
NM_001044385.3:c.1038-105C= MANE Select	NP_001037850.1:n.1038-105C=
NM_152388.4:c.1014-105C=	NP_689601.2:n.1014-105C=