Canonical Allele Identifier: CA1417731815

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773307G= , CM000665.2:g.165773307G=	GRCh38
NC_000003.11:g.165491095G= , CM000665.1:g.165491095G=	GRCh37
NC_000003.10:g.166973789G=	NCBI36
NG_009031.1:g.69159C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.*75C= MANE Select	ENSP00000264381.3:n.*75C=
ENST00000264381.7:c.*75C=	ENSP00000264381.3:n.*75C=
ENST00000479451.5:c.474C=	ENSP00000418325.1:n.474C=
ENST00000482958.1:c.*390C=	ENSP00000419804.1:n.*390C=
ENST00000497011.5:c.*274C=	ENSP00000419505.1:n.*274C=
NM_000055.2:c.*75C=	NP_000046.1:n.*75C=
XM_005247685.1:c.*75C=	XP_005247742.1:n.*75C=
NM_000055.3:c.*75C=	NP_000046.1:n.*75C=
NR_137635.1:n.526C=
NR_137636.1:n.2130C=
NM_000055.4:c.*75C= MANE Select	NP_000046.1:n.*75C=
NR_137635.2:n.477C=
NR_137636.2:n.2081C=