Canonical Allele Identifier: CA470841232

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797038A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037281A>C , CM000672.2:g.95037281A>C	GRCh38
NC_000010.10:g.96797038A>C , CM000672.1:g.96797038A>C	GRCh37
NC_000010.9:g.96787028A>C	NCBI36
NG_007972.1:g.37217T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1320T>G MANE Select	ENSP00000360317.3:p.Leu440=
ENST00000371270.5:c.1320T>G	ENSP00000360317.3:p.Leu440=
ENST00000490994.6:c.*1106T>G	ENSP00000433314.1:n.*1106T>G
ENST00000525991.5:c.*895T>G	ENSP00000433842.1:n.*895T>G
ENST00000526814.5:n.1575T>G
ENST00000527420.5:c.*177T>G	ENSP00000433191.1:n.*177T>G
ENST00000527953.5:n.1614T>G
ENST00000531714.1:n.508T>G
ENST00000533320.5:n.1554T>G
ENST00000535898.5:c.1014T>G	ENSP00000445062.1:p.Leu338=
ENST00000539050.5:c.1110T>G	ENSP00000442343.2:p.Leu370=
ENST00000623108.3:c.1110T>G	ENSP00000485110.1:p.Leu370=
NM_000770.3:c.1320T>G MANE Select	NP_000761.3:p.Leu440=
NM_001198853.1:c.1110T>G	NP_001185782.1:p.Leu370=
NM_001198854.1:c.1014T>G	NP_001185783.1:p.Leu338=
NM_001198855.1:c.1110T>G	NP_001185784.1:p.Leu370=
XR_945610.1:n.1455T>G