Canonical Allele Identifier: CA377677447

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796990A>C (hg19) ; chr10:g.95037233A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037233A>C , CM000672.2:g.95037233A>C	GRCh38
NC_000010.10:g.96796990A>C , CM000672.1:g.96796990A>C	GRCh37
NC_000010.9:g.96786980A>C	NCBI36
NG_007972.1:g.37265T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1368T>G MANE Select	ENSP00000360317.3:p.Phe456Leu
ENST00000371270.5:c.1368T>G	ENSP00000360317.3:p.Phe456Leu
ENST00000490994.6:c.*1154T>G	ENSP00000433314.1:n.*1154T>G
ENST00000525991.5:c.*943T>G	ENSP00000433842.1:n.*943T>G
ENST00000526814.5:n.1623T>G
ENST00000527420.5:c.*225T>G	ENSP00000433191.1:n.*225T>G
ENST00000527953.5:n.1662T>G
ENST00000531714.1:n.556T>G
ENST00000533320.5:n.1602T>G
ENST00000535898.5:c.1062T>G	ENSP00000445062.1:p.Phe354Leu
ENST00000539050.5:c.1158T>G	ENSP00000442343.2:p.Phe386Leu
ENST00000623108.3:c.1158T>G	ENSP00000485110.1:p.Phe386Leu
NM_000770.3:c.1368T>G MANE Select	NP_000761.3:p.Phe456Leu
NM_001198853.1:c.1158T>G	NP_001185782.1:p.Phe386Leu
NM_001198854.1:c.1062T>G	NP_001185783.1:p.Phe354Leu
NM_001198855.1:c.1158T>G	NP_001185784.1:p.Phe386Leu
XR_945610.1:n.1503T>G