Canonical Allele Identifier: CA1417731821

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773313T= , CM000665.2:g.165773313T=	GRCh38
NC_000003.11:g.165491101T= , CM000665.1:g.165491101T=	GRCh37
NC_000003.10:g.166973795T=	NCBI36
NG_009031.1:g.69153A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.*69A= MANE Select	ENSP00000264381.3:n.*69A=
ENST00000264381.7:c.*69A=	ENSP00000264381.3:n.*69A=
ENST00000479451.5:c.468A=	ENSP00000418325.1:n.468A=
ENST00000482958.1:c.*384A=	ENSP00000419804.1:n.*384A=
ENST00000497011.5:c.*268A=	ENSP00000419505.1:n.*268A=
NM_000055.2:c.*69A=	NP_000046.1:n.*69A=
XM_005247685.1:c.*69A=	XP_005247742.1:n.*69A=
NM_000055.3:c.*69A=	NP_000046.1:n.*69A=
NR_137635.1:n.520A=
NR_137636.1:n.2124A=
NM_000055.4:c.*69A= MANE Select	NP_000046.1:n.*69A=
NR_137635.2:n.471A=
NR_137636.2:n.2075A=