Canonical Allele Identifier: CA470841186

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796957G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037200G>A , CM000672.2:g.95037200G>A	GRCh38
NC_000010.10:g.96796957G>A , CM000672.1:g.96796957G>A	GRCh37
NC_000010.9:g.96786947G>A	NCBI36
NG_007972.1:g.37298C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1401C>T MANE Select	ENSP00000360317.3:p.Leu467=
ENST00000371270.5:c.1401C>T	ENSP00000360317.3:p.Leu467=
ENST00000490994.6:c.*1187C>T	ENSP00000433314.1:n.*1187C>T
ENST00000525991.5:c.*976C>T	ENSP00000433842.1:n.*976C>T
ENST00000526814.5:n.1656C>T
ENST00000527420.5:c.*258C>T	ENSP00000433191.1:n.*258C>T
ENST00000527953.5:n.1695C>T
ENST00000531714.1:n.589C>T
ENST00000533320.5:n.1635C>T
ENST00000535898.5:c.1095C>T	ENSP00000445062.1:p.Leu365=
ENST00000539050.5:c.1191C>T	ENSP00000442343.2:p.Leu397=
ENST00000623108.3:c.1191C>T	ENSP00000485110.1:p.Leu397=
NM_000770.3:c.1401C>T MANE Select	NP_000761.3:p.Leu467=
NM_001198853.1:c.1191C>T	NP_001185782.1:p.Leu397=
NM_001198854.1:c.1095C>T	NP_001185783.1:p.Leu365=
NM_001198855.1:c.1191C>T	NP_001185784.1:p.Leu397=
XR_945610.1:n.1536C>T