Canonical Allele Identifier: CA377677626

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96798657C>T (hg19) ; chr10:g.95038900C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038900C>T , CM000672.2:g.95038900C>T	GRCh38
NC_000010.10:g.96798657C>T , CM000672.1:g.96798657C>T	GRCh37
NC_000010.9:g.96788647C>T	NCBI36
NG_007972.1:g.35598G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1288G>A MANE Select	ENSP00000360317.3:p.Ala430Thr
ENST00000371270.5:c.1288G>A	ENSP00000360317.3:p.Ala430Thr
ENST00000490994.6:c.*1074G>A	ENSP00000433314.1:n.*1074G>A
ENST00000525991.5:c.*863G>A	ENSP00000433842.1:n.*863G>A
ENST00000526814.5:n.1543G>A
ENST00000527420.5:c.*145G>A	ENSP00000433191.1:n.*145G>A
ENST00000527953.5:n.1582G>A
ENST00000531714.1:n.476G>A
ENST00000533320.5:n.1522G>A
ENST00000535898.5:c.982G>A	ENSP00000445062.1:p.Ala328Thr
ENST00000539050.5:c.1078G>A	ENSP00000442343.2:p.Ala360Thr
ENST00000623108.3:c.1078G>A	ENSP00000485110.1:p.Ala360Thr
NM_000770.3:c.1288G>A MANE Select	NP_000761.3:p.Ala430Thr
NM_001198853.1:c.1078G>A	NP_001185782.1:p.Ala360Thr
NM_001198854.1:c.982G>A	NP_001185783.1:p.Ala328Thr
NM_001198855.1:c.1078G>A	NP_001185784.1:p.Ala360Thr
XR_945610.1:n.1423G>A