Canonical Allele Identifier: CA1417759828

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829995C= , CM000665.2:g.165829995C=	GRCh38
NC_000003.11:g.165547783C= , CM000665.1:g.165547783C=	GRCh37
NC_000003.10:g.167030477C=	NCBI36
NG_009031.1:g.12471G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1039G= MANE Select	ENSP00000264381.3:p.Val347=
ENST00000264381.7:c.1039G=	ENSP00000264381.3:p.Val347=
ENST00000479451.5:c.107+7319G=	ENSP00000418325.1:n.107+7319G=
ENST00000482958.1:c.1039G=	ENSP00000419804.1:p.Val347=
ENST00000488954.1:c.107+7319G=	ENSP00000418504.1:n.107+7319G=
ENST00000497011.5:c.1039G=	ENSP00000419505.1:p.Val347=
NM_000055.2:c.1039G=	NP_000046.1:p.Val347=
XM_005247685.1:c.1162G=	XP_005247742.1:p.Val388=
NM_000055.3:c.1039G=	NP_000046.1:p.Val347=
NR_137635.1:n.159+7319G=
NR_137636.1:n.1206G=
NM_000055.4:c.1039G= MANE Select	NP_000046.1:p.Val347=
NR_137635.2:n.110+7319G=
NR_137636.2:n.1157G=