Canonical Allele Identifier: CA1417764174

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165837239T= , CM000665.2:g.165837239T=	GRCh38
NC_000003.11:g.165555027T= , CM000665.1:g.165555027T=	GRCh37
NC_000003.10:g.167037721T=	NCBI36
NG_009031.1:g.5227A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.-9+75A= MANE Select	ENSP00000264381.3:n.-9+75A=
ENST00000264381.7:c.-9+75A=	ENSP00000264381.3:n.-9+75A=
ENST00000479451.5:c.107+75A=	ENSP00000418325.1:n.107+75A=
ENST00000482958.1:c.-9+75A=	ENSP00000419804.1:n.-9+75A=
ENST00000488954.1:c.107+75A=	ENSP00000418504.1:n.107+75A=
ENST00000497011.5:c.-9+75A=	ENSP00000419505.1:n.-9+75A=
NM_000055.2:c.-9+75A=	NP_000046.1:n.-9+75A=
XM_005247685.1:c.115+75A=	XP_005247742.1:n.115+75A=
NM_000055.3:c.-9+75A=	NP_000046.1:n.-9+75A=
NR_137635.1:n.159+75A=
NR_137636.1:n.159+75A=
NM_000055.4:c.-9+75A= MANE Select	NP_000046.1:n.-9+75A=
NR_137635.2:n.110+75A=
NR_137636.2:n.110+75A=