Canonical Allele Identifier: CA1929375441

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037272C= , CM000672.2:g.95037272C=	GRCh38
NC_000010.10:g.96797029C= , CM000672.1:g.96797029C=	GRCh37
NC_000010.9:g.96787019C=	NCBI36
NG_007972.1:g.37226G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1329G= MANE Select	ENSP00000360317.3:p.Met443=
ENST00000371270.5:c.1329G=	ENSP00000360317.3:p.Met443=
ENST00000490994.6:c.*1115G=	ENSP00000433314.1:n.*1115G=
ENST00000525991.5:c.*904G=	ENSP00000433842.1:n.*904G=
ENST00000526814.5:n.1584G=
ENST00000527420.5:c.*186G=	ENSP00000433191.1:n.*186G=
ENST00000527953.5:n.1623G=
ENST00000531714.1:n.517G=
ENST00000533320.5:n.1563G=
ENST00000535898.5:c.1023G=	ENSP00000445062.1:p.Met341=
ENST00000539050.5:c.1119G=	ENSP00000442343.2:p.Met373=
ENST00000623108.3:c.1119G=	ENSP00000485110.1:p.Met373=
NM_000770.3:c.1329G= MANE Select	NP_000761.3:p.Met443=
NM_001198853.1:c.1119G=	NP_001185782.1:p.Met373=
NM_001198854.1:c.1023G=	NP_001185783.1:p.Met341=
NM_001198855.1:c.1119G=	NP_001185784.1:p.Met373=
XR_945610.1:n.1464G=