Canonical Allele Identifier: CA1417711661

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786235T= , CM000665.2:g.165786235T=	GRCh38
NC_000003.11:g.165504023T= , CM000665.1:g.165504023T=	GRCh37
NC_000003.10:g.166986717T=	NCBI36
NG_009031.1:g.56231A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1594A= MANE Select	ENSP00000264381.3:p.Asn532=
ENST00000264381.7:c.1594A=	ENSP00000264381.3:p.Asn532=
ENST00000479451.5:c.184A=	ENSP00000418325.1:p.Asn62=
ENST00000482958.1:c.*100A=	ENSP00000419804.1:n.*100A=
ENST00000488954.1:c.184A=	ENSP00000418504.1:p.Asn62=
ENST00000497011.5:c.1594A=	ENSP00000419505.1:p.Asn532=
NM_000055.2:c.1594A=	NP_000046.1:p.Asn532=
XM_005247685.1:c.1717A=	XP_005247742.1:p.Asn573=
NM_000055.3:c.1594A=	NP_000046.1:p.Asn532=
NR_137635.1:n.236A=
NR_137636.1:n.1761A=
NM_000055.4:c.1594A= MANE Select	NP_000046.1:p.Asn532=
NR_137635.2:n.187A=
NR_137636.2:n.1712A=