Canonical Allele Identifier: CA1417760791

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830633T= , CM000665.2:g.165830633T=	GRCh38
NC_000003.11:g.165548421T= , CM000665.1:g.165548421T=	GRCh37
NC_000003.10:g.167031115T=	NCBI36
NG_009031.1:g.11833A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.401A= MANE Select	ENSP00000264381.3:p.Asn134=
ENST00000264381.7:c.401A=	ENSP00000264381.3:p.Asn134=
ENST00000479451.5:c.107+6681A=	ENSP00000418325.1:n.107+6681A=
ENST00000482958.1:c.401A=	ENSP00000419804.1:p.Asn134=
ENST00000488954.1:c.107+6681A=	ENSP00000418504.1:n.107+6681A=
ENST00000497011.5:c.401A=	ENSP00000419505.1:p.Asn134=
NM_000055.2:c.401A=	NP_000046.1:p.Asn134=
XM_005247685.1:c.524A=	XP_005247742.1:p.Asn175=
NM_000055.3:c.401A=	NP_000046.1:p.Asn134=
NR_137635.1:n.159+6681A=
NR_137636.1:n.568A=
NM_000055.4:c.401A= MANE Select	NP_000046.1:p.Asn134=
NR_137635.2:n.110+6681A=
NR_137636.2:n.519A=