Canonical Allele Identifier: CA5617474

Gene: CYP2C8

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037219_95037221del , CM000672.2:g.95037219_95037221del	GRCh38
NC_000010.10:g.96796976_96796978del , CM000672.1:g.96796976_96796978del	GRCh37
NC_000010.9:g.96786966_96786968del	NCBI36
NG_007972.1:g.37279_37281del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1382_1384del MANE Select	ENSP00000360317.3:p.Val461del
ENST00000371270.5:c.1382_1384del	ENSP00000360317.3:p.Val461del
ENST00000490994.6:c.*1168_*1170del	ENSP00000433314.1:n.*1168_*1170del
ENST00000525991.5:c.*957_*959del	ENSP00000433842.1:n.*957_*959del
ENST00000526814.5:n.1637_1639del
ENST00000527420.5:c.*239_*241del	ENSP00000433191.1:n.*239_*241del
ENST00000527953.5:n.1676_1678del
ENST00000531714.1:n.570_572del
ENST00000533320.5:n.1616_1618del
ENST00000535898.5:c.1076_1078del	ENSP00000445062.1:p.Val359del
ENST00000539050.5:c.1172_1174del	ENSP00000442343.2:p.Val391del
ENST00000623108.3:c.1172_1174del	ENSP00000485110.1:p.Val391del
NM_000770.3:c.1382_1384del MANE Select	NP_000761.3:p.Val461del
NM_001198853.1:c.1172_1174del	NP_001185782.1:p.Val391del
NM_001198854.1:c.1076_1078del	NP_001185783.1:p.Val359del
NM_001198855.1:c.1172_1174del	NP_001185784.1:p.Val391del
XR_945610.1:n.1517_1519del