Canonical Allele Identifier: CA470841153

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796921C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037164C>T , CM000672.2:g.95037164C>T	GRCh38
NC_000010.10:g.96796921C>T , CM000672.1:g.96796921C>T	GRCh37
NC_000010.9:g.96786911C>T	NCBI36
NG_007972.1:g.37334G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1437G>A MANE Select	ENSP00000360317.3:p.Leu479=
ENST00000371270.5:c.1437G>A	ENSP00000360317.3:p.Leu479=
ENST00000490994.6:c.*1223G>A	ENSP00000433314.1:n.*1223G>A
ENST00000525991.5:c.*1012G>A	ENSP00000433842.1:n.*1012G>A
ENST00000526814.5:n.1692G>A
ENST00000527420.5:c.*294G>A	ENSP00000433191.1:n.*294G>A
ENST00000527953.5:n.1731G>A
ENST00000533320.5:n.1671G>A
ENST00000535898.5:c.1131G>A	ENSP00000445062.1:p.Leu377=
ENST00000539050.5:c.1227G>A	ENSP00000442343.2:p.Leu409=
ENST00000623108.3:c.1227G>A	ENSP00000485110.1:p.Leu409=
NM_000770.3:c.1437G>A MANE Select	NP_000761.3:p.Leu479=
NM_001198853.1:c.1227G>A	NP_001185782.1:p.Leu409=
NM_001198854.1:c.1131G>A	NP_001185783.1:p.Leu377=
NM_001198855.1:c.1227G>A	NP_001185784.1:p.Leu409=