Canonical Allele Identifier: CA2789074757

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95051169G>T , CM000672.2:g.95051169G>T	GRCh38
NC_000010.10:g.96810926G>T , CM000672.1:g.96810926G>T	GRCh37
NC_000010.9:g.96800916G>T	NCBI36
NG_007972.1:g.23329C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.820-5218C>A MANE Select	ENSP00000360317.3:n.820-5218C>A
ENST00000371270.5:c.820-5218C>A	ENSP00000360317.3:n.820-5218C>A
ENST00000479946.2:n.1124-5218C>A
ENST00000490994.6:c.*606-5218C>A	ENSP00000433314.1:n.*606-5218C>A
ENST00000525991.5:c.*395-5218C>A	ENSP00000433842.1:n.*395-5218C>A
ENST00000526814.5:n.1075-5218C>A
ENST00000527420.5:c.820-5218C>A	ENSP00000433191.1:n.820-5218C>A
ENST00000527953.5:n.1075-5218C>A
ENST00000533320.5:n.1054-5218C>A
ENST00000535898.5:c.514-5218C>A	ENSP00000445062.1:n.514-5218C>A
ENST00000539050.5:c.610-5218C>A	ENSP00000442343.2:n.610-5218C>A
ENST00000623108.3:c.610-5218C>A	ENSP00000485110.1:n.610-5218C>A
ENST00000628935.1:c.562-5218C>A	ENSP00000487145.1:n.562-5218C>A
NM_000770.3:c.820-5218C>A MANE Select	NP_000761.3:n.820-5218C>A
NM_001198853.1:c.610-5218C>A	NP_001185782.1:n.610-5218C>A
NM_001198854.1:c.514-5218C>A	NP_001185783.1:n.514-5218C>A
NM_001198855.1:c.610-5218C>A	NP_001185784.1:n.610-5218C>A
XR_945610.1:n.916-5218C>A