Canonical Allele Identifier: CA1929375255

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037185A= , CM000672.2:g.95037185A=	GRCh38
NC_000010.10:g.96796942A= , CM000672.1:g.96796942A=	GRCh37
NC_000010.9:g.96786932A=	NCBI36
NG_007972.1:g.37313T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1416T= MANE Select	ENSP00000360317.3:p.Val472=
ENST00000371270.5:c.1416T=	ENSP00000360317.3:p.Val472=
ENST00000490994.6:c.*1202T=	ENSP00000433314.1:n.*1202T=
ENST00000525991.5:c.*991T=	ENSP00000433842.1:n.*991T=
ENST00000526814.5:n.1671T=
ENST00000527420.5:c.*273T=	ENSP00000433191.1:n.*273T=
ENST00000527953.5:n.1710T=
ENST00000531714.1:n.604T=
ENST00000533320.5:n.1650T=
ENST00000535898.5:c.1110T=	ENSP00000445062.1:p.Val370=
ENST00000539050.5:c.1206T=	ENSP00000442343.2:p.Val402=
ENST00000623108.3:c.1206T=	ENSP00000485110.1:p.Val402=
NM_000770.3:c.1416T= MANE Select	NP_000761.3:p.Val472=
NM_001198853.1:c.1206T=	NP_001185782.1:p.Val402=
NM_001198854.1:c.1110T=	NP_001185783.1:p.Val370=
NM_001198855.1:c.1206T=	NP_001185784.1:p.Val402=
XR_945610.1:n.1551T=