Canonical Allele Identifier: CA470841176

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796945T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037188T>A , CM000672.2:g.95037188T>A	GRCh38
NC_000010.10:g.96796945T>A , CM000672.1:g.96796945T>A	GRCh37
NC_000010.9:g.96786935T>A	NCBI36
NG_007972.1:g.37310A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1413A>T MANE Select	ENSP00000360317.3:p.Ala471=
ENST00000371270.5:c.1413A>T	ENSP00000360317.3:p.Ala471=
ENST00000490994.6:c.*1199A>T	ENSP00000433314.1:n.*1199A>T
ENST00000525991.5:c.*988A>T	ENSP00000433842.1:n.*988A>T
ENST00000526814.5:n.1668A>T
ENST00000527420.5:c.*270A>T	ENSP00000433191.1:n.*270A>T
ENST00000527953.5:n.1707A>T
ENST00000531714.1:n.601A>T
ENST00000533320.5:n.1647A>T
ENST00000535898.5:c.1107A>T	ENSP00000445062.1:p.Ala369=
ENST00000539050.5:c.1203A>T	ENSP00000442343.2:p.Ala401=
ENST00000623108.3:c.1203A>T	ENSP00000485110.1:p.Ala401=
NM_000770.3:c.1413A>T MANE Select	NP_000761.3:p.Ala471=
NM_001198853.1:c.1203A>T	NP_001185782.1:p.Ala401=
NM_001198854.1:c.1107A>T	NP_001185783.1:p.Ala369=
NM_001198855.1:c.1203A>T	NP_001185784.1:p.Ala401=
XR_945610.1:n.1548A>T