Canonical Allele Identifier: CA470841198

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796978A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037221A>C , CM000672.2:g.95037221A>C	GRCh38
NC_000010.10:g.96796978A>C , CM000672.1:g.96796978A>C	GRCh37
NC_000010.9:g.96786968A>C	NCBI36
NG_007972.1:g.37277T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1380T>G MANE Select	ENSP00000360317.3:p.Ser460=
ENST00000371270.5:c.1380T>G	ENSP00000360317.3:p.Ser460=
ENST00000490994.6:c.*1166T>G	ENSP00000433314.1:n.*1166T>G
ENST00000525991.5:c.*955T>G	ENSP00000433842.1:n.*955T>G
ENST00000526814.5:n.1635T>G
ENST00000527420.5:c.*237T>G	ENSP00000433191.1:n.*237T>G
ENST00000527953.5:n.1674T>G
ENST00000531714.1:n.568T>G
ENST00000533320.5:n.1614T>G
ENST00000535898.5:c.1074T>G	ENSP00000445062.1:p.Ser358=
ENST00000539050.5:c.1170T>G	ENSP00000442343.2:p.Ser390=
ENST00000623108.3:c.1170T>G	ENSP00000485110.1:p.Ser390=
NM_000770.3:c.1380T>G MANE Select	NP_000761.3:p.Ser460=
NM_001198853.1:c.1170T>G	NP_001185782.1:p.Ser390=
NM_001198854.1:c.1074T>G	NP_001185783.1:p.Ser358=
NM_001198855.1:c.1170T>G	NP_001185784.1:p.Ser390=
XR_945610.1:n.1515T>G