Canonical Allele Identifier: CA1417760038

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830140T= , CM000665.2:g.165830140T=	GRCh38
NC_000003.11:g.165547928T= , CM000665.1:g.165547928T=	GRCh37
NC_000003.10:g.167030622T=	NCBI36
NG_009031.1:g.12326A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.894A= MANE Select	ENSP00000264381.3:p.Gln298=
ENST00000264381.7:c.894A=	ENSP00000264381.3:p.Gln298=
ENST00000479451.5:c.107+7174A=	ENSP00000418325.1:n.107+7174A=
ENST00000482958.1:c.894A=	ENSP00000419804.1:p.Gln298=
ENST00000488954.1:c.107+7174A=	ENSP00000418504.1:n.107+7174A=
ENST00000497011.5:c.894A=	ENSP00000419505.1:p.Gln298=
NM_000055.2:c.894A=	NP_000046.1:p.Gln298=
XM_005247685.1:c.1017A=	XP_005247742.1:p.Gln339=
NM_000055.3:c.894A=	NP_000046.1:p.Gln298=
NR_137635.1:n.159+7174A=
NR_137636.1:n.1061A=
NM_000055.4:c.894A= MANE Select	NP_000046.1:p.Gln298=
NR_137635.2:n.110+7174A=
NR_137636.2:n.1012A=