Canonical Allele Identifier: CA377677499

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797014A>C (hg19) ; chr10:g.95037257A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037257A>C , CM000672.2:g.95037257A>C	GRCh38
NC_000010.10:g.96797014A>C , CM000672.1:g.96797014A>C	GRCh37
NC_000010.9:g.96787004A>C	NCBI36
NG_007972.1:g.37241T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1344T>G MANE Select	ENSP00000360317.3:p.Phe448Leu
ENST00000371270.5:c.1344T>G	ENSP00000360317.3:p.Phe448Leu
ENST00000490994.6:c.*1130T>G	ENSP00000433314.1:n.*1130T>G
ENST00000525991.5:c.*919T>G	ENSP00000433842.1:n.*919T>G
ENST00000526814.5:n.1599T>G
ENST00000527420.5:c.*201T>G	ENSP00000433191.1:n.*201T>G
ENST00000527953.5:n.1638T>G
ENST00000531714.1:n.532T>G
ENST00000533320.5:n.1578T>G
ENST00000535898.5:c.1038T>G	ENSP00000445062.1:p.Phe346Leu
ENST00000539050.5:c.1134T>G	ENSP00000442343.2:p.Phe378Leu
ENST00000623108.3:c.1134T>G	ENSP00000485110.1:p.Phe378Leu
NM_000770.3:c.1344T>G MANE Select	NP_000761.3:p.Phe448Leu
NM_001198853.1:c.1134T>G	NP_001185782.1:p.Phe378Leu
NM_001198854.1:c.1038T>G	NP_001185783.1:p.Phe346Leu
NM_001198855.1:c.1134T>G	NP_001185784.1:p.Phe378Leu
XR_945610.1:n.1479T>G