Canonical Allele Identifier: CA377677623

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96798656G>A (hg19) ; chr10:g.95038899G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038899G>A , CM000672.2:g.95038899G>A	GRCh38
NC_000010.10:g.96798656G>A , CM000672.1:g.96798656G>A	GRCh37
NC_000010.9:g.96788646G>A	NCBI36
NG_007972.1:g.35599C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1289C>T MANE Select	ENSP00000360317.3:p.Ala430Val
ENST00000371270.5:c.1289C>T	ENSP00000360317.3:p.Ala430Val
ENST00000490994.6:c.*1075C>T	ENSP00000433314.1:n.*1075C>T
ENST00000525991.5:c.*864C>T	ENSP00000433842.1:n.*864C>T
ENST00000526814.5:n.1544C>T
ENST00000527420.5:c.*146C>T	ENSP00000433191.1:n.*146C>T
ENST00000527953.5:n.1583C>T
ENST00000531714.1:n.477C>T
ENST00000533320.5:n.1523C>T
ENST00000535898.5:c.983C>T	ENSP00000445062.1:p.Ala328Val
ENST00000539050.5:c.1079C>T	ENSP00000442343.2:p.Ala360Val
ENST00000623108.3:c.1079C>T	ENSP00000485110.1:p.Ala360Val
NM_000770.3:c.1289C>T MANE Select	NP_000761.3:p.Ala430Val
NM_001198853.1:c.1079C>T	NP_001185782.1:p.Ala360Val
NM_001198854.1:c.983C>T	NP_001185783.1:p.Ala328Val
NM_001198855.1:c.1079C>T	NP_001185784.1:p.Ala360Val
XR_945610.1:n.1424C>T