Canonical Allele Identifier: CA377677513

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797019A>T (hg19) ; chr10:g.95037262A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037262A>T , CM000672.2:g.95037262A>T	GRCh38
NC_000010.10:g.96797019A>T , CM000672.1:g.96797019A>T	GRCh37
NC_000010.9:g.96787009A>T	NCBI36
NG_007972.1:g.37236T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1339T>A MANE Select	ENSP00000360317.3:p.Leu447Ile
ENST00000371270.5:c.1339T>A	ENSP00000360317.3:p.Leu447Ile
ENST00000490994.6:c.*1125T>A	ENSP00000433314.1:n.*1125T>A
ENST00000525991.5:c.*914T>A	ENSP00000433842.1:n.*914T>A
ENST00000526814.5:n.1594T>A
ENST00000527420.5:c.*196T>A	ENSP00000433191.1:n.*196T>A
ENST00000527953.5:n.1633T>A
ENST00000531714.1:n.527T>A
ENST00000533320.5:n.1573T>A
ENST00000535898.5:c.1033T>A	ENSP00000445062.1:p.Leu345Ile
ENST00000539050.5:c.1129T>A	ENSP00000442343.2:p.Leu377Ile
ENST00000623108.3:c.1129T>A	ENSP00000485110.1:p.Leu377Ile
NM_000770.3:c.1339T>A MANE Select	NP_000761.3:p.Leu447Ile
NM_001198853.1:c.1129T>A	NP_001185782.1:p.Leu377Ile
NM_001198854.1:c.1033T>A	NP_001185783.1:p.Leu345Ile
NM_001198855.1:c.1129T>A	NP_001185784.1:p.Leu377Ile
XR_945610.1:n.1474T>A