Canonical Allele Identifier: CA1417760777

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830601C= , CM000665.2:g.165830601C=	GRCh38
NC_000003.11:g.165548389C= , CM000665.1:g.165548389C=	GRCh37
NC_000003.10:g.167031083C=	NCBI36
NG_009031.1:g.11865G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.433G= MANE Select	ENSP00000264381.3:p.Gly145=
ENST00000264381.7:c.433G=	ENSP00000264381.3:p.Gly145=
ENST00000479451.5:c.107+6713G=	ENSP00000418325.1:n.107+6713G=
ENST00000482958.1:c.433G=	ENSP00000419804.1:p.Gly145=
ENST00000488954.1:c.107+6713G=	ENSP00000418504.1:n.107+6713G=
ENST00000497011.5:c.433G=	ENSP00000419505.1:p.Gly145=
NM_000055.2:c.433G=	NP_000046.1:p.Gly145=
XM_005247685.1:c.556G=	XP_005247742.1:p.Gly186=
NM_000055.3:c.433G=	NP_000046.1:p.Gly145=
NR_137635.1:n.159+6713G=
NR_137636.1:n.600G=
NM_000055.4:c.433G= MANE Select	NP_000046.1:p.Gly145=
NR_137635.2:n.110+6713G=
NR_137636.2:n.551G=