Canonical Allele Identifier: CA1417732152

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773498C= , CM000665.2:g.165773498C=	GRCh38
NC_000003.11:g.165491286C= , CM000665.1:g.165491286C=	GRCh37
NC_000003.10:g.166973980C=	NCBI36
NG_009031.1:g.68968G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1693G= MANE Select	ENSP00000264381.3:p.Asp565=
ENST00000264381.7:c.1693G=	ENSP00000264381.3:p.Asp565=
ENST00000479451.5:c.283G=	ENSP00000418325.1:p.Asp95=
ENST00000482958.1:c.*199G=	ENSP00000419804.1:n.*199G=
ENST00000497011.5:c.*83G=	ENSP00000419505.1:n.*83G=
NM_000055.2:c.1693G=	NP_000046.1:p.Asp565=
XM_005247685.1:c.1816G=	XP_005247742.1:p.Asp606=
NM_000055.3:c.1693G=	NP_000046.1:p.Asp565=
NR_137635.1:n.335G=
NR_137636.1:n.1939G=
NM_000055.4:c.1693G= MANE Select	NP_000046.1:p.Asp565=
NR_137635.2:n.286G=
NR_137636.2:n.1890G=