Canonical Allele Identifier: CA377677325

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796934C>A (hg19) ; chr10:g.95037177C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037177C>A , CM000672.2:g.95037177C>A	GRCh38
NC_000010.10:g.96796934C>A , CM000672.1:g.96796934C>A	GRCh37
NC_000010.9:g.96786924C>A	NCBI36
NG_007972.1:g.37321G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1424G>T MANE Select	ENSP00000360317.3:p.Gly475Val
ENST00000371270.5:c.1424G>T	ENSP00000360317.3:p.Gly475Val
ENST00000490994.6:c.*1210G>T	ENSP00000433314.1:n.*1210G>T
ENST00000525991.5:c.*999G>T	ENSP00000433842.1:n.*999G>T
ENST00000526814.5:n.1679G>T
ENST00000527420.5:c.*281G>T	ENSP00000433191.1:n.*281G>T
ENST00000527953.5:n.1718G>T
ENST00000533320.5:n.1658G>T
ENST00000535898.5:c.1118G>T	ENSP00000445062.1:p.Gly373Val
ENST00000539050.5:c.1214G>T	ENSP00000442343.2:p.Gly405Val
ENST00000623108.3:c.1214G>T	ENSP00000485110.1:p.Gly405Val
NM_000770.3:c.1424G>T MANE Select	NP_000761.3:p.Gly475Val
NM_001198853.1:c.1214G>T	NP_001185782.1:p.Gly405Val
NM_001198854.1:c.1118G>T	NP_001185783.1:p.Gly373Val
NM_001198855.1:c.1214G>T	NP_001185784.1:p.Gly405Val
XR_945610.1:n.1559G>T