Canonical Allele Identifier: CA653612201

Gene: CYP2C8

Linked Data

• COSMIC: COSN1124746

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037049_95037064del , CM000672.2:g.95037049_95037064del	GRCh38
NC_000010.10:g.96796806_96796821del , CM000672.1:g.96796806_96796821del	GRCh37
NC_000010.9:g.96786796_96786811del	NCBI36
NG_007972.1:g.37437_37452del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*67_*82del MANE Select	ENSP00000360317.3:n.*67_*82del
ENST00000371270.5:c.*67_*82del	ENSP00000360317.3:n.*67_*82del
ENST00000490994.6:c.*1326_*1341del	ENSP00000433314.1:n.*1326_*1341del
ENST00000525991.5:c.*1115_*1130del	ENSP00000433842.1:n.*1115_*1130del
ENST00000526814.5:n.1795_1810del
ENST00000527420.5:c.*397_*412del	ENSP00000433191.1:n.*397_*412del
ENST00000527953.5:n.1834_1849del
ENST00000533320.5:n.1774_1789del
ENST00000535898.5:c.*67_*82del	ENSP00000445062.1:n.*67_*82del
ENST00000539050.5:c.*67_*82del	ENSP00000442343.2:n.*67_*82del
ENST00000623108.3:c.*67_*82del	ENSP00000485110.1:n.*67_*82del
NM_000770.3:c.*67_*82del MANE Select	NP_000761.3:n.*67_*82del
NM_001198853.1:c.*67_*82del	NP_001185782.1:n.*67_*82del
NM_001198854.1:c.*67_*82del	NP_001185783.1:n.*67_*82del
NM_001198855.1:c.*67_*82del	NP_001185784.1:n.*67_*82del