Canonical Allele Identifier: CA377677352

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037190-C-T
• MyVariant Identifiers: chr10:g.96796947C>T (hg19) ; chr10:g.95037190C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037190C>T , CM000672.2:g.95037190C>T	GRCh38
NC_000010.10:g.96796947C>T , CM000672.1:g.96796947C>T	GRCh37
NC_000010.9:g.96786937C>T	NCBI36
NG_007972.1:g.37308G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1411G>A MANE Select	ENSP00000360317.3:p.Ala471Thr
ENST00000371270.5:c.1411G>A	ENSP00000360317.3:p.Ala471Thr
ENST00000490994.6:c.*1197G>A	ENSP00000433314.1:n.*1197G>A
ENST00000525991.5:c.*986G>A	ENSP00000433842.1:n.*986G>A
ENST00000526814.5:n.1666G>A
ENST00000527420.5:c.*268G>A	ENSP00000433191.1:n.*268G>A
ENST00000527953.5:n.1705G>A
ENST00000531714.1:n.599G>A
ENST00000533320.5:n.1645G>A
ENST00000535898.5:c.1105G>A	ENSP00000445062.1:p.Ala369Thr
ENST00000539050.5:c.1201G>A	ENSP00000442343.2:p.Ala401Thr
ENST00000623108.3:c.1201G>A	ENSP00000485110.1:p.Ala401Thr
NM_000770.3:c.1411G>A MANE Select	NP_000761.3:p.Ala471Thr
NM_001198853.1:c.1201G>A	NP_001185782.1:p.Ala401Thr
NM_001198854.1:c.1105G>A	NP_001185783.1:p.Ala369Thr
NM_001198855.1:c.1201G>A	NP_001185784.1:p.Ala401Thr
XR_945610.1:n.1546G>A