Canonical Allele Identifier: CA1417731812

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773303A= , CM000665.2:g.165773303A=	GRCh38
NC_000003.11:g.165491091A= , CM000665.1:g.165491091A=	GRCh37
NC_000003.10:g.166973785A=	NCBI36
NG_009031.1:g.69163T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.*79T= MANE Select	ENSP00000264381.3:n.*79T=
ENST00000264381.7:c.*79T=	ENSP00000264381.3:n.*79T=
ENST00000479451.5:c.478T=	ENSP00000418325.1:n.478T=
ENST00000482958.1:c.*394T=	ENSP00000419804.1:n.*394T=
ENST00000497011.5:c.*278T=	ENSP00000419505.1:n.*278T=
NM_000055.2:c.*79T=	NP_000046.1:n.*79T=
XM_005247685.1:c.*79T=	XP_005247742.1:n.*79T=
NM_000055.3:c.*79T=	NP_000046.1:n.*79T=
NR_137635.1:n.530T=
NR_137636.1:n.2134T=
NM_000055.4:c.*79T= MANE Select	NP_000046.1:n.*79T=
NR_137635.2:n.481T=
NR_137636.2:n.2085T=