Canonical Allele Identifier: CA1417732161

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773504T= , CM000665.2:g.165773504T=	GRCh38
NC_000003.11:g.165491292T= , CM000665.1:g.165491292T=	GRCh37
NC_000003.10:g.166973986T=	NCBI36
NG_009031.1:g.68962A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1687A= MANE Select	ENSP00000264381.3:p.Asn563=
ENST00000264381.7:c.1687A=	ENSP00000264381.3:p.Asn563=
ENST00000479451.5:c.277A=	ENSP00000418325.1:p.Asn93=
ENST00000482958.1:c.*193A=	ENSP00000419804.1:n.*193A=
ENST00000497011.5:c.*77A=	ENSP00000419505.1:n.*77A=
NM_000055.2:c.1687A=	NP_000046.1:p.Asn563=
XM_005247685.1:c.1810A=	XP_005247742.1:p.Asn604=
NM_000055.3:c.1687A=	NP_000046.1:p.Asn563=
NR_137635.1:n.329A=
NR_137636.1:n.1933A=
NM_000055.4:c.1687A= MANE Select	NP_000046.1:p.Asn563=
NR_137635.2:n.280A=
NR_137636.2:n.1884A=