Canonical Allele Identifier: CA1929375194

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037163G= , CM000672.2:g.95037163G=	GRCh38
NC_000010.10:g.96796920G= , CM000672.1:g.96796920G=	GRCh37
NC_000010.9:g.96786910G=	NCBI36
NG_007972.1:g.37335C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1438C= MANE Select	ENSP00000360317.3:p.Pro480=
ENST00000371270.5:c.1438C=	ENSP00000360317.3:p.Pro480=
ENST00000490994.6:c.*1224C=	ENSP00000433314.1:n.*1224C=
ENST00000525991.5:c.*1013C=	ENSP00000433842.1:n.*1013C=
ENST00000526814.5:n.1693C=
ENST00000527420.5:c.*295C=	ENSP00000433191.1:n.*295C=
ENST00000527953.5:n.1732C=
ENST00000533320.5:n.1672C=
ENST00000535898.5:c.1132C=	ENSP00000445062.1:p.Pro378=
ENST00000539050.5:c.1228C=	ENSP00000442343.2:p.Pro410=
ENST00000623108.3:c.1228C=	ENSP00000485110.1:p.Pro410=
NM_000770.3:c.1438C= MANE Select	NP_000761.3:p.Pro480=
NM_001198853.1:c.1228C=	NP_001185782.1:p.Pro410=
NM_001198854.1:c.1132C=	NP_001185783.1:p.Pro378=
NM_001198855.1:c.1228C=	NP_001185784.1:p.Pro410=