Canonical Allele Identifier: CA377679371

Gene: CYP2C8

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95058349T>G , CM000672.2:g.95058349T>G	GRCh38
NC_000010.10:g.96818106T>G , CM000672.1:g.96818106T>G	GRCh37
NC_000010.9:g.96808096T>G	NCBI36
NG_007972.1:g.16149A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.805A>C MANE Select	ENSP00000360317.3:p.Ile269Leu
ENST00000371270.5:c.805A>C	ENSP00000360317.3:p.Ile269Leu
ENST00000479946.2:n.1109A>C
ENST00000490994.6:c.*591A>C	ENSP00000433314.1:n.*591A>C
ENST00000525991.5:c.*380A>C	ENSP00000433842.1:n.*380A>C
ENST00000526814.5:n.1060A>C
ENST00000527420.5:c.805A>C	ENSP00000433191.1:p.Ile269Leu
ENST00000527953.5:n.1060A>C
ENST00000533320.5:n.1039A>C
ENST00000535898.5:c.499A>C	ENSP00000445062.1:p.Ile167Leu
ENST00000539050.5:c.595A>C	ENSP00000442343.2:p.Ile199Leu
ENST00000623108.3:c.595A>C	ENSP00000485110.1:p.Ile199Leu
ENST00000628935.1:c.547A>C	ENSP00000487145.1:p.Ile183Leu
NM_000770.3:c.805A>C MANE Select	NP_000761.3:p.Ile269Leu
NM_001198853.1:c.595A>C	NP_001185782.1:p.Ile199Leu
NM_001198854.1:c.499A>C	NP_001185783.1:p.Ile167Leu
NM_001198855.1:c.595A>C	NP_001185784.1:p.Ile199Leu
XR_945610.1:n.901A>C