Canonical Allele Identifier: CA377677374

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796959G>A (hg19) ; chr10:g.95037202G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037202G>A , CM000672.2:g.95037202G>A	GRCh38
NC_000010.10:g.96796959G>A , CM000672.1:g.96796959G>A	GRCh37
NC_000010.9:g.96786949G>A	NCBI36
NG_007972.1:g.37296C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1399C>T MANE Select	ENSP00000360317.3:p.Leu467Phe
ENST00000371270.5:c.1399C>T	ENSP00000360317.3:p.Leu467Phe
ENST00000490994.6:c.*1185C>T	ENSP00000433314.1:n.*1185C>T
ENST00000525991.5:c.*974C>T	ENSP00000433842.1:n.*974C>T
ENST00000526814.5:n.1654C>T
ENST00000527420.5:c.*256C>T	ENSP00000433191.1:n.*256C>T
ENST00000527953.5:n.1693C>T
ENST00000531714.1:n.587C>T
ENST00000533320.5:n.1633C>T
ENST00000535898.5:c.1093C>T	ENSP00000445062.1:p.Leu365Phe
ENST00000539050.5:c.1189C>T	ENSP00000442343.2:p.Leu397Phe
ENST00000623108.3:c.1189C>T	ENSP00000485110.1:p.Leu397Phe
NM_000770.3:c.1399C>T MANE Select	NP_000761.3:p.Leu467Phe
NM_001198853.1:c.1189C>T	NP_001185782.1:p.Leu397Phe
NM_001198854.1:c.1093C>T	NP_001185783.1:p.Leu365Phe
NM_001198855.1:c.1189C>T	NP_001185784.1:p.Leu397Phe
XR_945610.1:n.1534C>T