Canonical Allele Identifier: CA355113800

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165491188T>A (hg19) ; chr3:g.165773400T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773400T>A , CM000665.2:g.165773400T>A	GRCh38
NC_000003.11:g.165491188T>A , CM000665.1:g.165491188T>A	GRCh37
NC_000003.10:g.166973882T>A	NCBI36
NG_009031.1:g.69066A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1791A>T MANE Select	ENSP00000264381.3:p.Glu597Asp
ENST00000264381.7:c.1791A>T	ENSP00000264381.3:p.Glu597Asp
ENST00000479451.5:c.381A>T	ENSP00000418325.1:p.Glu127Asp
ENST00000482958.1:c.*297A>T	ENSP00000419804.1:n.*297A>T
ENST00000497011.5:c.*181A>T	ENSP00000419505.1:n.*181A>T
NM_000055.2:c.1791A>T	NP_000046.1:p.Glu597Asp
XM_005247685.1:c.1914A>T	XP_005247742.1:p.Glu638Asp
NM_000055.3:c.1791A>T	NP_000046.1:p.Glu597Asp
NR_137635.1:n.433A>T
NR_137636.1:n.2037A>T
NM_000055.4:c.1791A>T MANE Select	NP_000046.1:p.Glu597Asp
NR_137635.2:n.384A>T
NR_137636.2:n.1988A>T