Canonical Allele Identifier: CA377677484

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797006G>C (hg19) ; chr10:g.95037249G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037249G>C , CM000672.2:g.95037249G>C	GRCh38
NC_000010.10:g.96797006G>C , CM000672.1:g.96797006G>C	GRCh37
NC_000010.9:g.96786996G>C	NCBI36
NG_007972.1:g.37249C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1352C>G MANE Select	ENSP00000360317.3:p.Thr451Arg
ENST00000371270.5:c.1352C>G	ENSP00000360317.3:p.Thr451Arg
ENST00000490994.6:c.*1138C>G	ENSP00000433314.1:n.*1138C>G
ENST00000525991.5:c.*927C>G	ENSP00000433842.1:n.*927C>G
ENST00000526814.5:n.1607C>G
ENST00000527420.5:c.*209C>G	ENSP00000433191.1:n.*209C>G
ENST00000527953.5:n.1646C>G
ENST00000531714.1:n.540C>G
ENST00000533320.5:n.1586C>G
ENST00000535898.5:c.1046C>G	ENSP00000445062.1:p.Thr349Arg
ENST00000539050.5:c.1142C>G	ENSP00000442343.2:p.Thr381Arg
ENST00000623108.3:c.1142C>G	ENSP00000485110.1:p.Thr381Arg
NM_000770.3:c.1352C>G MANE Select	NP_000761.3:p.Thr451Arg
NM_001198853.1:c.1142C>G	NP_001185782.1:p.Thr381Arg
NM_001198854.1:c.1046C>G	NP_001185783.1:p.Thr349Arg
NM_001198855.1:c.1142C>G	NP_001185784.1:p.Thr381Arg
XR_945610.1:n.1487C>G