Canonical Allele Identifier: CA1417711795

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786311C= , CM000665.2:g.165786311C=	GRCh38
NC_000003.11:g.165504099C= , CM000665.1:g.165504099C=	GRCh37
NC_000003.10:g.166986793C=	NCBI36
NG_009031.1:g.56155G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1518G= MANE Select	ENSP00000264381.3:p.Gly506=
ENST00000264381.7:c.1518G=	ENSP00000264381.3:p.Gly506=
ENST00000479451.5:c.108G=	ENSP00000418325.1:p.Gly36=
ENST00000482958.1:c.*24G=	ENSP00000419804.1:n.*24G=
ENST00000488954.1:c.108G=	ENSP00000418504.1:p.Gly36=
ENST00000497011.5:c.1518G=	ENSP00000419505.1:p.Gly506=
NM_000055.2:c.1518G=	NP_000046.1:p.Gly506=
XM_005247685.1:c.1641G=	XP_005247742.1:p.Gly547=
NM_000055.3:c.1518G=	NP_000046.1:p.Gly506=
NR_137635.1:n.160G=
NR_137636.1:n.1685G=
NM_000055.4:c.1518G= MANE Select	NP_000046.1:p.Gly506=
NR_137635.2:n.111G=
NR_137636.2:n.1636G=