Canonical Allele Identifier: CA377683119

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95067309-G-A
• COSMIC: COSM5929178 ; COSM5929179 ; COSM5929180
• MyVariant Identifiers: chr10:g.96827066G>A (hg19) ; chr10:g.95067309G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067309G>A , CM000672.2:g.95067309G>A	GRCh38
NC_000010.10:g.96827066G>A , CM000672.1:g.96827066G>A	GRCh37
NC_000010.9:g.96817056G>A	NCBI36
NG_007972.1:g.7189C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.380C>T MANE Select	ENSP00000360317.3:p.Ser127Phe
ENST00000371270.5:c.380C>T	ENSP00000360317.3:p.Ser127Phe
ENST00000479946.2:n.684C>T
ENST00000490994.6:c.*166C>T	ENSP00000433314.1:n.*166C>T
ENST00000525991.5:c.255C>T	ENSP00000433842.1:p.Leu85=
ENST00000526814.5:n.635C>T
ENST00000527420.5:c.380C>T	ENSP00000433191.1:p.Ser127Phe
ENST00000527953.5:n.635C>T
ENST00000533320.5:n.614C>T
ENST00000535898.5:c.74C>T	ENSP00000445062.1:p.Ser25Phe
ENST00000539050.5:c.170C>T	ENSP00000442343.2:p.Ser57Phe
ENST00000623108.3:c.170C>T	ENSP00000485110.1:p.Ser57Phe
ENST00000628935.1:c.122C>T	ENSP00000487145.1:p.Ser41Phe
NM_000770.3:c.380C>T MANE Select	NP_000761.3:p.Ser127Phe
NM_001198853.1:c.170C>T	NP_001185782.1:p.Ser57Phe
NM_001198854.1:c.74C>T	NP_001185783.1:p.Ser25Phe
NM_001198855.1:c.170C>T	NP_001185784.1:p.Ser57Phe
XR_945610.1:n.476C>T