Canonical Allele Identifier: CA1929375354

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037225T= , CM000672.2:g.95037225T=	GRCh38
NC_000010.10:g.96796982T= , CM000672.1:g.96796982T=	GRCh37
NC_000010.9:g.96786972T=	NCBI36
NG_007972.1:g.37273A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1376A= MANE Select	ENSP00000360317.3:p.Lys459=
ENST00000371270.5:c.1376A=	ENSP00000360317.3:p.Lys459=
ENST00000490994.6:c.*1162A=	ENSP00000433314.1:n.*1162A=
ENST00000525991.5:c.*951A=	ENSP00000433842.1:n.*951A=
ENST00000526814.5:n.1631A=
ENST00000527420.5:c.*233A=	ENSP00000433191.1:n.*233A=
ENST00000527953.5:n.1670A=
ENST00000531714.1:n.564A=
ENST00000533320.5:n.1610A=
ENST00000535898.5:c.1070A=	ENSP00000445062.1:p.Lys357=
ENST00000539050.5:c.1166A=	ENSP00000442343.2:p.Lys389=
ENST00000623108.3:c.1166A=	ENSP00000485110.1:p.Lys389=
NM_000770.3:c.1376A= MANE Select	NP_000761.3:p.Lys459=
NM_001198853.1:c.1166A=	NP_001185782.1:p.Lys389=
NM_001198854.1:c.1070A=	NP_001185783.1:p.Lys357=
NM_001198855.1:c.1166A=	NP_001185784.1:p.Lys389=
XR_945610.1:n.1511A=