Canonical Allele Identifier: CA377683280

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827105G>T (hg19) ; chr10:g.95067348G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067348G>T , CM000672.2:g.95067348G>T	GRCh38
NC_000010.10:g.96827105G>T , CM000672.1:g.96827105G>T	GRCh37
NC_000010.9:g.96817095G>T	NCBI36
NG_007972.1:g.7150C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.341C>A MANE Select	ENSP00000360317.3:p.Ser114Tyr
ENST00000371270.5:c.341C>A	ENSP00000360317.3:p.Ser114Tyr
ENST00000479946.2:n.645C>A
ENST00000490994.6:c.*127C>A	ENSP00000433314.1:n.*127C>A
ENST00000525991.5:c.216C>A	ENSP00000433842.1:p.Phe72Leu
ENST00000526814.5:n.596C>A
ENST00000527420.5:c.341C>A	ENSP00000433191.1:p.Ser114Tyr
ENST00000527953.5:n.596C>A
ENST00000533320.5:n.575C>A
ENST00000535898.5:c.35C>A	ENSP00000445062.1:p.Ser12Tyr
ENST00000539050.5:c.131C>A	ENSP00000442343.2:p.Ser44Tyr
ENST00000623108.3:c.131C>A	ENSP00000485110.1:p.Ser44Tyr
ENST00000628935.1:c.83C>A	ENSP00000487145.1:p.Ser28Tyr
NM_000770.3:c.341C>A MANE Select	NP_000761.3:p.Ser114Tyr
NM_001198853.1:c.131C>A	NP_001185782.1:p.Ser44Tyr
NM_001198854.1:c.35C>A	NP_001185783.1:p.Ser12Tyr
NM_001198855.1:c.131C>A	NP_001185784.1:p.Ser44Tyr
XR_945610.1:n.437C>A