Canonical Allele Identifier: CA470841243

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797050T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037293T>A , CM000672.2:g.95037293T>A	GRCh38
NC_000010.10:g.96797050T>A , CM000672.1:g.96797050T>A	GRCh37
NC_000010.9:g.96787040T>A	NCBI36
NG_007972.1:g.37205A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1308A>T MANE Select	ENSP00000360317.3:p.Ala436=
ENST00000371270.5:c.1308A>T	ENSP00000360317.3:p.Ala436=
ENST00000490994.6:c.*1094A>T	ENSP00000433314.1:n.*1094A>T
ENST00000525991.5:c.*883A>T	ENSP00000433842.1:n.*883A>T
ENST00000526814.5:n.1563A>T
ENST00000527420.5:c.*165A>T	ENSP00000433191.1:n.*165A>T
ENST00000527953.5:n.1602A>T
ENST00000531714.1:n.496A>T
ENST00000533320.5:n.1542A>T
ENST00000535898.5:c.1002A>T	ENSP00000445062.1:p.Ala334=
ENST00000539050.5:c.1098A>T	ENSP00000442343.2:p.Ala366=
ENST00000623108.3:c.1098A>T	ENSP00000485110.1:p.Ala366=
NM_000770.3:c.1308A>T MANE Select	NP_000761.3:p.Ala436=
NM_001198853.1:c.1098A>T	NP_001185782.1:p.Ala366=
NM_001198854.1:c.1002A>T	NP_001185783.1:p.Ala334=
NM_001198855.1:c.1098A>T	NP_001185784.1:p.Ala366=
XR_945610.1:n.1443A>T