Canonical Allele Identifier: CA355114207

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165491282T>G (hg19) ; chr3:g.165773494T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773494T>G , CM000665.2:g.165773494T>G	GRCh38
NC_000003.11:g.165491282T>G , CM000665.1:g.165491282T>G	GRCh37
NC_000003.10:g.166973976T>G	NCBI36
NG_009031.1:g.68972A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1697A>C MANE Select	ENSP00000264381.3:p.Glu566Ala
ENST00000264381.7:c.1697A>C	ENSP00000264381.3:p.Glu566Ala
ENST00000479451.5:c.287A>C	ENSP00000418325.1:p.Glu96Ala
ENST00000482958.1:c.*203A>C	ENSP00000419804.1:n.*203A>C
ENST00000497011.5:c.*87A>C	ENSP00000419505.1:n.*87A>C
NM_000055.2:c.1697A>C	NP_000046.1:p.Glu566Ala
XM_005247685.1:c.1820A>C	XP_005247742.1:p.Glu607Ala
NM_000055.3:c.1697A>C	NP_000046.1:p.Glu566Ala
NR_137635.1:n.339A>C
NR_137636.1:n.1943A>C
NM_000055.4:c.1697A>C MANE Select	NP_000046.1:p.Glu566Ala
NR_137635.2:n.290A>C
NR_137636.2:n.1894A>C