Canonical Allele Identifier: CA2789074430

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037053_95037054del , CM000672.2:g.95037053_95037054del	GRCh38
NC_000010.10:g.96796810_96796811del , CM000672.1:g.96796810_96796811del	GRCh37
NC_000010.9:g.96786800_96786801del	NCBI36
NG_007972.1:g.37445_37446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*75_*76del MANE Select	ENSP00000360317.3:n.*75_*76del
ENST00000371270.5:c.*75_*76del	ENSP00000360317.3:n.*75_*76del
ENST00000490994.6:c.*1334_*1335del	ENSP00000433314.1:n.*1334_*1335del
ENST00000525991.5:c.*1123_*1124del	ENSP00000433842.1:n.*1123_*1124del
ENST00000526814.5:n.1803_1804del
ENST00000527420.5:c.*405_*406del	ENSP00000433191.1:n.*405_*406del
ENST00000527953.5:n.1842_1843del
ENST00000533320.5:n.1782_1783del
ENST00000535898.5:c.*75_*76del	ENSP00000445062.1:n.*75_*76del
ENST00000539050.5:c.*75_*76del	ENSP00000442343.2:n.*75_*76del
ENST00000623108.3:c.*75_*76del	ENSP00000485110.1:n.*75_*76del
NM_000770.3:c.*75_*76del MANE Select	NP_000761.3:n.*75_*76del
NM_001198853.1:c.*75_*76del	NP_001185782.1:n.*75_*76del
NM_001198854.1:c.*75_*76del	NP_001185783.1:n.*75_*76del
NM_001198855.1:c.*75_*76del	NP_001185784.1:n.*75_*76del