Canonical Allele Identifier: CA1929375319

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037216_95037219delinsTCAA , CM000672.2:g.95037216_95037219delinsTCAA	GRCh38
NC_000010.10:g.96796973_96796976delinsTCAA , CM000672.1:g.96796973_96796976delinsTCAA	GRCh37
NC_000010.9:g.96786963_96786966delinsTCAA	NCBI36
NG_007972.1:g.37279_37282delinsTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1382_1385delinsTTGA MANE Select	ENSP00000360317.3:p.Val461=
ENST00000371270.5:c.1382_1385delinsTTGA	ENSP00000360317.3:p.Val461=
ENST00000490994.6:c.*1168_*1171delinsTTGA	ENSP00000433314.1:n.*1168_*1171delinsTTGA
ENST00000525991.5:c.*957_*960delinsTTGA	ENSP00000433842.1:n.*957_*960delinsTTGA
ENST00000526814.5:n.1637_1640delinsTTGA
ENST00000527420.5:c.*239_*242delinsTTGA	ENSP00000433191.1:n.*239_*242delinsTTGA
ENST00000527953.5:n.1676_1679delinsTTGA
ENST00000531714.1:n.570_573delinsTTGA
ENST00000533320.5:n.1616_1619delinsTTGA
ENST00000535898.5:c.1076_1079delinsTTGA	ENSP00000445062.1:p.Val359=
ENST00000539050.5:c.1172_1175delinsTTGA	ENSP00000442343.2:p.Val391=
ENST00000623108.3:c.1172_1175delinsTTGA	ENSP00000485110.1:p.Val391=
NM_000770.3:c.1382_1385delinsTTGA MANE Select	NP_000761.3:p.Val461=
NM_001198853.1:c.1172_1175delinsTTGA	NP_001185782.1:p.Val391=
NM_001198854.1:c.1076_1079delinsTTGA	NP_001185783.1:p.Val359=
NM_001198855.1:c.1172_1175delinsTTGA	NP_001185784.1:p.Val391=
XR_945610.1:n.1517_1520delinsTTGA