Canonical Allele Identifier: CA377677531

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797027T>G (hg19) ; chr10:g.95037270T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037270T>G , CM000672.2:g.95037270T>G	GRCh38
NC_000010.10:g.96797027T>G , CM000672.1:g.96797027T>G	GRCh37
NC_000010.9:g.96787017T>G	NCBI36
NG_007972.1:g.37228A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1331A>C MANE Select	ENSP00000360317.3:p.Glu444Ala
ENST00000371270.5:c.1331A>C	ENSP00000360317.3:p.Glu444Ala
ENST00000490994.6:c.*1117A>C	ENSP00000433314.1:n.*1117A>C
ENST00000525991.5:c.*906A>C	ENSP00000433842.1:n.*906A>C
ENST00000526814.5:n.1586A>C
ENST00000527420.5:c.*188A>C	ENSP00000433191.1:n.*188A>C
ENST00000527953.5:n.1625A>C
ENST00000531714.1:n.519A>C
ENST00000533320.5:n.1565A>C
ENST00000535898.5:c.1025A>C	ENSP00000445062.1:p.Glu342Ala
ENST00000539050.5:c.1121A>C	ENSP00000442343.2:p.Glu374Ala
ENST00000623108.3:c.1121A>C	ENSP00000485110.1:p.Glu374Ala
NM_000770.3:c.1331A>C MANE Select	NP_000761.3:p.Glu444Ala
NM_001198853.1:c.1121A>C	NP_001185782.1:p.Glu374Ala
NM_001198854.1:c.1025A>C	NP_001185783.1:p.Glu342Ala
NM_001198855.1:c.1121A>C	NP_001185784.1:p.Glu374Ala
XR_945610.1:n.1466A>C