Canonical Allele Identifier: CA1417760979

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165831052G= , CM000665.2:g.165831052G=	GRCh38
NC_000003.11:g.165548840G= , CM000665.1:g.165548840G=	GRCh37
NC_000003.10:g.167031534G=	NCBI36
NG_009031.1:g.11414C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.-8-11C= MANE Select	ENSP00000264381.3:n.-8-11C=
ENST00000264381.7:c.-8-11C=	ENSP00000264381.3:n.-8-11C=
ENST00000479451.5:c.107+6262C=	ENSP00000418325.1:n.107+6262C=
ENST00000482958.1:c.-8-11C=	ENSP00000419804.1:n.-8-11C=
ENST00000488954.1:c.107+6262C=	ENSP00000418504.1:n.107+6262C=
ENST00000497011.5:c.-8-11C=	ENSP00000419505.1:n.-8-11C=
NM_000055.2:c.-8-11C=	NP_000046.1:n.-8-11C=
XM_005247685.1:c.116-11C=	XP_005247742.1:n.116-11C=
NM_000055.3:c.-8-11C=	NP_000046.1:n.-8-11C=
NR_137635.1:n.159+6262C=
NR_137636.1:n.160-11C=
NM_000055.4:c.-8-11C= MANE Select	NP_000046.1:n.-8-11C=
NR_137635.2:n.110+6262C=
NR_137636.2:n.111-11C=