Canonical Allele Identifier: CA1417760266

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830275T= , CM000665.2:g.165830275T=	GRCh38
NC_000003.11:g.165548063T= , CM000665.1:g.165548063T=	GRCh37
NC_000003.10:g.167030757T=	NCBI36
NG_009031.1:g.12191A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.759A= MANE Select	ENSP00000264381.3:p.Gly253=
ENST00000264381.7:c.759A=	ENSP00000264381.3:p.Gly253=
ENST00000479451.5:c.107+7039A=	ENSP00000418325.1:n.107+7039A=
ENST00000482958.1:c.759A=	ENSP00000419804.1:p.Gly253=
ENST00000488954.1:c.107+7039A=	ENSP00000418504.1:n.107+7039A=
ENST00000497011.5:c.759A=	ENSP00000419505.1:p.Gly253=
NM_000055.2:c.759A=	NP_000046.1:p.Gly253=
XM_005247685.1:c.882A=	XP_005247742.1:p.Gly294=
NM_000055.3:c.759A=	NP_000046.1:p.Gly253=
NR_137635.1:n.159+7039A=
NR_137636.1:n.926A=
NM_000055.4:c.759A= MANE Select	NP_000046.1:p.Gly253=
NR_137635.2:n.110+7039A=
NR_137636.2:n.877A=