Canonical Allele Identifier: CA1321143698

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623464A= , CM000664.2:g.201623464A=	GRCh38
NC_000002.11:g.202488187A= , CM000664.1:g.202488187A=	GRCh37
NC_000002.10:g.202196432A=	NCBI36
NG_032049.1:g.25066T=
NG_051007.1:g.719T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*791T=	ENSP00000480508.2:n.*791T=
ENST00000686475.1:n.1958T=
ENST00000409883.7:c.*791T= MANE Select	ENSP00000386264.2:n.*791T=
ENST00000409444.6:c.*791T=	ENSP00000387203.2:n.*791T=
ENST00000409883.6:c.*791T=	ENSP00000386264.2:n.*791T=
ENST00000495329.1:n.1157T=
NM_001044385.2:c.*791T=	NP_001037850.1:n.*791T=
NM_152388.3:c.*791T=	NP_689601.2:n.*791T=
NM_001044385.3:c.*791T= MANE Select	NP_001037850.1:n.*791T=
NM_152388.4:c.*791T=	NP_689601.2:n.*791T=