Canonical Allele Identifier: CA470841219

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797013G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037256G>A , CM000672.2:g.95037256G>A	GRCh38
NC_000010.10:g.96797013G>A , CM000672.1:g.96797013G>A	GRCh37
NC_000010.9:g.96787003G>A	NCBI36
NG_007972.1:g.37242C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1345C>T MANE Select	ENSP00000360317.3:p.Leu449=
ENST00000371270.5:c.1345C>T	ENSP00000360317.3:p.Leu449=
ENST00000490994.6:c.*1131C>T	ENSP00000433314.1:n.*1131C>T
ENST00000525991.5:c.*920C>T	ENSP00000433842.1:n.*920C>T
ENST00000526814.5:n.1600C>T
ENST00000527420.5:c.*202C>T	ENSP00000433191.1:n.*202C>T
ENST00000527953.5:n.1639C>T
ENST00000531714.1:n.533C>T
ENST00000533320.5:n.1579C>T
ENST00000535898.5:c.1039C>T	ENSP00000445062.1:p.Leu347=
ENST00000539050.5:c.1135C>T	ENSP00000442343.2:p.Leu379=
ENST00000623108.3:c.1135C>T	ENSP00000485110.1:p.Leu379=
NM_000770.3:c.1345C>T MANE Select	NP_000761.3:p.Leu449=
NM_001198853.1:c.1135C>T	NP_001185782.1:p.Leu379=
NM_001198854.1:c.1039C>T	NP_001185783.1:p.Leu347=
NM_001198855.1:c.1135C>T	NP_001185784.1:p.Leu379=
XR_945610.1:n.1480C>T