Canonical Allele Identifier: CA470841203

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796984C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037227C>T , CM000672.2:g.95037227C>T	GRCh38
NC_000010.10:g.96796984C>T , CM000672.1:g.96796984C>T	GRCh37
NC_000010.9:g.96786974C>T	NCBI36
NG_007972.1:g.37271G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1374G>A MANE Select	ENSP00000360317.3:p.Leu458=
ENST00000371270.5:c.1374G>A	ENSP00000360317.3:p.Leu458=
ENST00000490994.6:c.*1160G>A	ENSP00000433314.1:n.*1160G>A
ENST00000525991.5:c.*949G>A	ENSP00000433842.1:n.*949G>A
ENST00000526814.5:n.1629G>A
ENST00000527420.5:c.*231G>A	ENSP00000433191.1:n.*231G>A
ENST00000527953.5:n.1668G>A
ENST00000531714.1:n.562G>A
ENST00000533320.5:n.1608G>A
ENST00000535898.5:c.1068G>A	ENSP00000445062.1:p.Leu356=
ENST00000539050.5:c.1164G>A	ENSP00000442343.2:p.Leu388=
ENST00000623108.3:c.1164G>A	ENSP00000485110.1:p.Leu388=
NM_000770.3:c.1374G>A MANE Select	NP_000761.3:p.Leu458=
NM_001198853.1:c.1164G>A	NP_001185782.1:p.Leu388=
NM_001198854.1:c.1068G>A	NP_001185783.1:p.Leu356=
NM_001198855.1:c.1164G>A	NP_001185784.1:p.Leu388=
XR_945610.1:n.1509G>A