Canonical Allele Identifier: CA1417732087

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773470C= , CM000665.2:g.165773470C=	GRCh38
NC_000003.11:g.165491258C= , CM000665.1:g.165491258C=	GRCh37
NC_000003.10:g.166973952C=	NCBI36
NG_009031.1:g.68996G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1721G= MANE Select	ENSP00000264381.3:p.Gly574=
ENST00000264381.7:c.1721G=	ENSP00000264381.3:p.Gly574=
ENST00000479451.5:c.311G=	ENSP00000418325.1:p.Gly104=
ENST00000482958.1:c.*227G=	ENSP00000419804.1:n.*227G=
ENST00000497011.5:c.*111G=	ENSP00000419505.1:n.*111G=
NM_000055.2:c.1721G=	NP_000046.1:p.Gly574=
XM_005247685.1:c.1844G=	XP_005247742.1:p.Gly615=
NM_000055.3:c.1721G=	NP_000046.1:p.Gly574=
NR_137635.1:n.363G=
NR_137636.1:n.1967G=
NM_000055.4:c.1721G= MANE Select	NP_000046.1:p.Gly574=
NR_137635.2:n.314G=
NR_137636.2:n.1918G=