Canonical Allele Identifier: CA1929388147

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067212G= , CM000672.2:g.95067212G=	GRCh38
NC_000010.10:g.96826969G= , CM000672.1:g.96826969G=	GRCh37
NC_000010.9:g.96816959G=	NCBI36
NG_007972.1:g.7286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.477C= MANE Select	ENSP00000360317.3:p.Thr159=
ENST00000371270.5:c.477C=	ENSP00000360317.3:p.Thr159=
ENST00000479946.2:n.781C=
ENST00000490994.6:c.*263C=	ENSP00000433314.1:n.*263C=
ENST00000525991.5:c.*52C=	ENSP00000433842.1:n.*52C=
ENST00000526814.5:n.732C=
ENST00000527420.5:c.477C=	ENSP00000433191.1:p.Thr159=
ENST00000527953.5:n.732C=
ENST00000533320.5:n.711C=
ENST00000535898.5:c.171C=	ENSP00000445062.1:p.Thr57=
ENST00000539050.5:c.267C=	ENSP00000442343.2:p.Thr89=
ENST00000623108.3:c.267C=	ENSP00000485110.1:p.Thr89=
ENST00000628935.1:c.219C=	ENSP00000487145.1:p.Thr73=
NM_000770.3:c.477C= MANE Select	NP_000761.3:p.Thr159=
NM_001198853.1:c.267C=	NP_001185782.1:p.Thr89=
NM_001198854.1:c.171C=	NP_001185783.1:p.Thr57=
NM_001198855.1:c.267C=	NP_001185784.1:p.Thr89=
XR_945610.1:n.573C=