Canonical Allele Identifier: CA470841137

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796891A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037134A>T , CM000672.2:g.95037134A>T	GRCh38
NC_000010.10:g.96796891A>T , CM000672.1:g.96796891A>T	GRCh37
NC_000010.9:g.96786881A>T	NCBI36
NG_007972.1:g.37364T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1467T>A MANE Select	ENSP00000360317.3:p.Pro489=
ENST00000371270.5:c.1467T>A	ENSP00000360317.3:p.Pro489=
ENST00000490994.6:c.*1253T>A	ENSP00000433314.1:n.*1253T>A
ENST00000525991.5:c.*1042T>A	ENSP00000433842.1:n.*1042T>A
ENST00000526814.5:n.1722T>A
ENST00000527420.5:c.*324T>A	ENSP00000433191.1:n.*324T>A
ENST00000527953.5:n.1761T>A
ENST00000533320.5:n.1701T>A
ENST00000535898.5:c.1161T>A	ENSP00000445062.1:p.Pro387=
ENST00000539050.5:c.1257T>A	ENSP00000442343.2:p.Pro419=
ENST00000623108.3:c.1257T>A	ENSP00000485110.1:p.Pro419=
NM_000770.3:c.1467T>A MANE Select	NP_000761.3:p.Pro489=
NM_001198853.1:c.1257T>A	NP_001185782.1:p.Pro419=
NM_001198854.1:c.1161T>A	NP_001185783.1:p.Pro387=
NM_001198855.1:c.1257T>A	NP_001185784.1:p.Pro419=