Canonical Allele Identifier: CA1417760051

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830153T= , CM000665.2:g.165830153T=	GRCh38
NC_000003.11:g.165547941T= , CM000665.1:g.165547941T=	GRCh37
NC_000003.10:g.167030635T=	NCBI36
NG_009031.1:g.12313A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.881A= MANE Select	ENSP00000264381.3:p.Asn294=
ENST00000264381.7:c.881A=	ENSP00000264381.3:p.Asn294=
ENST00000479451.5:c.107+7161A=	ENSP00000418325.1:n.107+7161A=
ENST00000482958.1:c.881A=	ENSP00000419804.1:p.Asn294=
ENST00000488954.1:c.107+7161A=	ENSP00000418504.1:n.107+7161A=
ENST00000497011.5:c.881A=	ENSP00000419505.1:p.Asn294=
NM_000055.2:c.881A=	NP_000046.1:p.Asn294=
XM_005247685.1:c.1004A=	XP_005247742.1:p.Asn335=
NM_000055.3:c.881A=	NP_000046.1:p.Asn294=
NR_137635.1:n.159+7161A=
NR_137636.1:n.1048A=
NM_000055.4:c.881A= MANE Select	NP_000046.1:p.Asn294=
NR_137635.2:n.110+7161A=
NR_137636.2:n.999A=