Canonical Allele Identifier: CA470841266

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96798661G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038904G>A , CM000672.2:g.95038904G>A	GRCh38
NC_000010.10:g.96798661G>A , CM000672.1:g.96798661G>A	GRCh37
NC_000010.9:g.96788651G>A	NCBI36
NG_007972.1:g.35594C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1284C>T MANE Select	ENSP00000360317.3:p.Phe428=
ENST00000371270.5:c.1284C>T	ENSP00000360317.3:p.Phe428=
ENST00000490994.6:c.*1070C>T	ENSP00000433314.1:n.*1070C>T
ENST00000525991.5:c.*859C>T	ENSP00000433842.1:n.*859C>T
ENST00000526814.5:n.1539C>T
ENST00000527420.5:c.*141C>T	ENSP00000433191.1:n.*141C>T
ENST00000527953.5:n.1578C>T
ENST00000531714.1:n.472C>T
ENST00000533320.5:n.1518C>T
ENST00000535898.5:c.978C>T	ENSP00000445062.1:p.Phe326=
ENST00000539050.5:c.1074C>T	ENSP00000442343.2:p.Phe358=
ENST00000623108.3:c.1074C>T	ENSP00000485110.1:p.Phe358=
NM_000770.3:c.1284C>T MANE Select	NP_000761.3:p.Phe428=
NM_001198853.1:c.1074C>T	NP_001185782.1:p.Phe358=
NM_001198854.1:c.978C>T	NP_001185783.1:p.Phe326=
NM_001198855.1:c.1074C>T	NP_001185784.1:p.Phe358=
XR_945610.1:n.1419C>T