Canonical Allele Identifier: CA377677619

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96798654C>G (hg19) ; chr10:g.95038897C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038897C>G , CM000672.2:g.95038897C>G	GRCh38
NC_000010.10:g.96798654C>G , CM000672.1:g.96798654C>G	GRCh37
NC_000010.9:g.96788644C>G	NCBI36
NG_007972.1:g.35601G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1291G>C MANE Select	ENSP00000360317.3:p.Gly431Arg
ENST00000371270.5:c.1291G>C	ENSP00000360317.3:p.Gly431Arg
ENST00000490994.6:c.*1077G>C	ENSP00000433314.1:n.*1077G>C
ENST00000525991.5:c.*866G>C	ENSP00000433842.1:n.*866G>C
ENST00000526814.5:n.1546G>C
ENST00000527420.5:c.*148G>C	ENSP00000433191.1:n.*148G>C
ENST00000527953.5:n.1585G>C
ENST00000531714.1:n.479G>C
ENST00000533320.5:n.1525G>C
ENST00000535898.5:c.985G>C	ENSP00000445062.1:p.Gly329Arg
ENST00000539050.5:c.1081G>C	ENSP00000442343.2:p.Gly361Arg
ENST00000623108.3:c.1081G>C	ENSP00000485110.1:p.Gly361Arg
NM_000770.3:c.1291G>C MANE Select	NP_000761.3:p.Gly431Arg
NM_001198853.1:c.1081G>C	NP_001185782.1:p.Gly361Arg
NM_001198854.1:c.985G>C	NP_001185783.1:p.Gly329Arg
NM_001198855.1:c.1081G>C	NP_001185784.1:p.Gly361Arg
XR_945610.1:n.1426G>C