Canonical Allele Identifier: CA1417711703

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786255T= , CM000665.2:g.165786255T=	GRCh38
NC_000003.11:g.165504043T= , CM000665.1:g.165504043T=	GRCh37
NC_000003.10:g.166986737T=	NCBI36
NG_009031.1:g.56211A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1574A= MANE Select	ENSP00000264381.3:p.Glu525=
ENST00000264381.7:c.1574A=	ENSP00000264381.3:p.Glu525=
ENST00000479451.5:c.164A=	ENSP00000418325.1:p.Glu55=
ENST00000482958.1:c.*80A=	ENSP00000419804.1:n.*80A=
ENST00000488954.1:c.164A=	ENSP00000418504.1:p.Glu55=
ENST00000497011.5:c.1574A=	ENSP00000419505.1:p.Glu525=
NM_000055.2:c.1574A=	NP_000046.1:p.Glu525=
XM_005247685.1:c.1697A=	XP_005247742.1:p.Glu566=
NM_000055.3:c.1574A=	NP_000046.1:p.Glu525=
NR_137635.1:n.216A=
NR_137636.1:n.1741A=
NM_000055.4:c.1574A= MANE Select	NP_000046.1:p.Glu525=
NR_137635.2:n.167A=
NR_137636.2:n.1692A=