Canonical Allele Identifier: CA1417731865

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773344T= , CM000665.2:g.165773344T=	GRCh38
NC_000003.11:g.165491132T= , CM000665.1:g.165491132T=	GRCh37
NC_000003.10:g.166973826T=	NCBI36
NG_009031.1:g.69122A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.*38A= MANE Select	ENSP00000264381.3:n.*38A=
ENST00000264381.7:c.*38A=	ENSP00000264381.3:n.*38A=
ENST00000479451.5:c.437A=	ENSP00000418325.1:n.437A=
ENST00000482958.1:c.*353A=	ENSP00000419804.1:n.*353A=
ENST00000497011.5:c.*237A=	ENSP00000419505.1:n.*237A=
NM_000055.2:c.*38A=	NP_000046.1:n.*38A=
XM_005247685.1:c.*38A=	XP_005247742.1:n.*38A=
NM_000055.3:c.*38A=	NP_000046.1:n.*38A=
NR_137635.1:n.489A=
NR_137636.1:n.2093A=
NM_000055.4:c.*38A= MANE Select	NP_000046.1:n.*38A=
NR_137635.2:n.440A=
NR_137636.2:n.2044A=