Canonical Allele Identifier: CA1929359218

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95040817A= , CM000672.2:g.95040817A=	GRCh38
NC_000010.10:g.96800574A= , CM000672.1:g.96800574A=	GRCh37
NC_000010.9:g.96790564A=	NCBI36
NG_007972.1:g.33681T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1150-1779T= MANE Select	ENSP00000360317.3:n.1150-1779T=
ENST00000371270.5:c.1150-1779T=	ENSP00000360317.3:n.1150-1779T=
ENST00000479946.2:n.1492+105T=
ENST00000490994.6:c.*936-1779T=	ENSP00000433314.1:n.*936-1779T=
ENST00000525991.5:c.*725-1779T=	ENSP00000433842.1:n.*725-1779T=
ENST00000526814.5:n.1405-1779T=
ENST00000527420.5:c.*6+105T=	ENSP00000433191.1:n.*6+105T=
ENST00000527953.5:n.1443+105T=
ENST00000533320.5:n.1384-1779T=
ENST00000535898.5:c.844-1779T=	ENSP00000445062.1:n.844-1779T=
ENST00000539050.5:c.940-1779T=	ENSP00000442343.2:n.940-1779T=
ENST00000623108.3:c.940-1779T=	ENSP00000485110.1:n.940-1779T=
NM_000770.3:c.1150-1779T= MANE Select	NP_000761.3:n.1150-1779T=
NM_001198853.1:c.940-1779T=	NP_001185782.1:n.940-1779T=
NM_001198854.1:c.844-1779T=	NP_001185783.1:n.844-1779T=
NM_001198855.1:c.940-1779T=	NP_001185784.1:n.940-1779T=
XR_945610.1:n.1284+105T=