Canonical Allele Identifier: CA377677422

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796979G>T (hg19) ; chr10:g.95037222G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037222G>T , CM000672.2:g.95037222G>T	GRCh38
NC_000010.10:g.96796979G>T , CM000672.1:g.96796979G>T	GRCh37
NC_000010.9:g.96786969G>T	NCBI36
NG_007972.1:g.37276C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1379C>A MANE Select	ENSP00000360317.3:p.Ser460Tyr
ENST00000371270.5:c.1379C>A	ENSP00000360317.3:p.Ser460Tyr
ENST00000490994.6:c.*1165C>A	ENSP00000433314.1:n.*1165C>A
ENST00000525991.5:c.*954C>A	ENSP00000433842.1:n.*954C>A
ENST00000526814.5:n.1634C>A
ENST00000527420.5:c.*236C>A	ENSP00000433191.1:n.*236C>A
ENST00000527953.5:n.1673C>A
ENST00000531714.1:n.567C>A
ENST00000533320.5:n.1613C>A
ENST00000535898.5:c.1073C>A	ENSP00000445062.1:p.Ser358Tyr
ENST00000539050.5:c.1169C>A	ENSP00000442343.2:p.Ser390Tyr
ENST00000623108.3:c.1169C>A	ENSP00000485110.1:p.Ser390Tyr
NM_000770.3:c.1379C>A MANE Select	NP_000761.3:p.Ser460Tyr
NM_001198853.1:c.1169C>A	NP_001185782.1:p.Ser390Tyr
NM_001198854.1:c.1073C>A	NP_001185783.1:p.Ser358Tyr
NM_001198855.1:c.1169C>A	NP_001185784.1:p.Ser390Tyr
XR_945610.1:n.1514C>A