Canonical Allele Identifier: CA1929375293

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037198T= , CM000672.2:g.95037198T=	GRCh38
NC_000010.10:g.96796955T= , CM000672.1:g.96796955T=	GRCh37
NC_000010.9:g.96786945T=	NCBI36
NG_007972.1:g.37300A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1403A= MANE Select	ENSP00000360317.3:p.Asn468=
ENST00000371270.5:c.1403A=	ENSP00000360317.3:p.Asn468=
ENST00000490994.6:c.*1189A=	ENSP00000433314.1:n.*1189A=
ENST00000525991.5:c.*978A=	ENSP00000433842.1:n.*978A=
ENST00000526814.5:n.1658A=
ENST00000527420.5:c.*260A=	ENSP00000433191.1:n.*260A=
ENST00000527953.5:n.1697A=
ENST00000531714.1:n.591A=
ENST00000533320.5:n.1637A=
ENST00000535898.5:c.1097A=	ENSP00000445062.1:p.Asn366=
ENST00000539050.5:c.1193A=	ENSP00000442343.2:p.Asn398=
ENST00000623108.3:c.1193A=	ENSP00000485110.1:p.Asn398=
NM_000770.3:c.1403A= MANE Select	NP_000761.3:p.Asn468=
NM_001198853.1:c.1193A=	NP_001185782.1:p.Asn398=
NM_001198854.1:c.1097A=	NP_001185783.1:p.Asn366=
NM_001198855.1:c.1193A=	NP_001185784.1:p.Asn398=
XR_945610.1:n.1538A=