Canonical Allele Identifier: CA377677317

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796929C>G (hg19) ; chr10:g.95037172C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037172C>G , CM000672.2:g.95037172C>G	GRCh38
NC_000010.10:g.96796929C>G , CM000672.1:g.96796929C>G	GRCh37
NC_000010.9:g.96786919C>G	NCBI36
NG_007972.1:g.37326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1429G>C MANE Select	ENSP00000360317.3:p.Val477Leu
ENST00000371270.5:c.1429G>C	ENSP00000360317.3:p.Val477Leu
ENST00000490994.6:c.*1215G>C	ENSP00000433314.1:n.*1215G>C
ENST00000525991.5:c.*1004G>C	ENSP00000433842.1:n.*1004G>C
ENST00000526814.5:n.1684G>C
ENST00000527420.5:c.*286G>C	ENSP00000433191.1:n.*286G>C
ENST00000527953.5:n.1723G>C
ENST00000533320.5:n.1663G>C
ENST00000535898.5:c.1123G>C	ENSP00000445062.1:p.Val375Leu
ENST00000539050.5:c.1219G>C	ENSP00000442343.2:p.Val407Leu
ENST00000623108.3:c.1219G>C	ENSP00000485110.1:p.Val407Leu
NM_000770.3:c.1429G>C MANE Select	NP_000761.3:p.Val477Leu
NM_001198853.1:c.1219G>C	NP_001185782.1:p.Val407Leu
NM_001198854.1:c.1123G>C	NP_001185783.1:p.Val375Leu
NM_001198855.1:c.1219G>C	NP_001185784.1:p.Val407Leu
XR_945610.1:n.1564G>C