Canonical Allele Identifier: CA377677582

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797054C>T (hg19) ; chr10:g.95037297C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037297C>T , CM000672.2:g.95037297C>T	GRCh38
NC_000010.10:g.96797054C>T , CM000672.1:g.96797054C>T	GRCh37
NC_000010.9:g.96787044C>T	NCBI36
NG_007972.1:g.37201G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1304G>A MANE Select	ENSP00000360317.3:p.Cys435Tyr
ENST00000371270.5:c.1304G>A	ENSP00000360317.3:p.Cys435Tyr
ENST00000490994.6:c.*1090G>A	ENSP00000433314.1:n.*1090G>A
ENST00000525991.5:c.*879G>A	ENSP00000433842.1:n.*879G>A
ENST00000526814.5:n.1559G>A
ENST00000527420.5:c.*161G>A	ENSP00000433191.1:n.*161G>A
ENST00000527953.5:n.1598G>A
ENST00000531714.1:n.492G>A
ENST00000533320.5:n.1538G>A
ENST00000535898.5:c.998G>A	ENSP00000445062.1:p.Cys333Tyr
ENST00000539050.5:c.1094G>A	ENSP00000442343.2:p.Cys365Tyr
ENST00000623108.3:c.1094G>A	ENSP00000485110.1:p.Cys365Tyr
NM_000770.3:c.1304G>A MANE Select	NP_000761.3:p.Cys435Tyr
NM_001198853.1:c.1094G>A	NP_001185782.1:p.Cys365Tyr
NM_001198854.1:c.998G>A	NP_001185783.1:p.Cys333Tyr
NM_001198855.1:c.1094G>A	NP_001185784.1:p.Cys365Tyr
XR_945610.1:n.1439G>A