Canonical Allele Identifier: CA1417731698

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773193C= , CM000665.2:g.165773193C=	GRCh38
NC_000003.11:g.165490981C= , CM000665.1:g.165490981C=	GRCh37
NC_000003.10:g.166973675C=	NCBI36
NG_009031.1:g.69273G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.*189G= MANE Select	ENSP00000264381.3:n.*189G=
ENST00000264381.7:c.*189G=	ENSP00000264381.3:n.*189G=
ENST00000479451.5:c.588G=	ENSP00000418325.1:n.588G=
ENST00000482958.1:c.*504G=	ENSP00000419804.1:n.*504G=
ENST00000497011.5:c.*388G=	ENSP00000419505.1:n.*388G=
NM_000055.2:c.*189G=	NP_000046.1:n.*189G=
XM_005247685.1:c.*189G=	XP_005247742.1:n.*189G=
NM_000055.3:c.*189G=	NP_000046.1:n.*189G=
NR_137635.1:n.640G=
NR_137636.1:n.2244G=
NM_000055.4:c.*189G= MANE Select	NP_000046.1:n.*189G=
NR_137635.2:n.591G=
NR_137636.2:n.2195G=