Canonical Allele Identifier: CA1417760201

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830246G= , CM000665.2:g.165830246G=	GRCh38
NC_000003.11:g.165548034G= , CM000665.1:g.165548034G=	GRCh37
NC_000003.10:g.167030728G=	NCBI36
NG_009031.1:g.12220C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.788C= MANE Select	ENSP00000264381.3:p.Ser263=
ENST00000264381.7:c.788C=	ENSP00000264381.3:p.Ser263=
ENST00000479451.5:c.107+7068C=	ENSP00000418325.1:n.107+7068C=
ENST00000482958.1:c.788C=	ENSP00000419804.1:p.Ser263=
ENST00000488954.1:c.107+7068C=	ENSP00000418504.1:n.107+7068C=
ENST00000497011.5:c.788C=	ENSP00000419505.1:p.Ser263=
NM_000055.2:c.788C=	NP_000046.1:p.Ser263=
XM_005247685.1:c.911C=	XP_005247742.1:p.Ser304=
NM_000055.3:c.788C=	NP_000046.1:p.Ser263=
NR_137635.1:n.159+7068C=
NR_137636.1:n.955C=
NM_000055.4:c.788C= MANE Select	NP_000046.1:p.Ser263=
NR_137635.2:n.110+7068C=
NR_137636.2:n.906C=