Canonical Allele Identifier: CA1929375493

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037300_95037302delinsATT , CM000672.2:g.95037300_95037302delinsATT	GRCh38
NC_000010.10:g.96797057_96797059delinsATT , CM000672.1:g.96797057_96797059delinsATT	GRCh37
NC_000010.9:g.96787047_96787049delinsATT	NCBI36
NG_007972.1:g.37196_37198delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1299_1301delinsAAT MANE Select	ENSP00000360317.3:p.Arg433=
ENST00000371270.5:c.1299_1301delinsAAT	ENSP00000360317.3:p.Arg433=
ENST00000490994.6:c.*1085_*1087delinsAAT	ENSP00000433314.1:n.*1085_*1087delinsAAT
ENST00000525991.5:c.*874_*876delinsAAT	ENSP00000433842.1:n.*874_*876delinsAAT
ENST00000526814.5:n.1554_1556delinsAAT
ENST00000527420.5:c.*156_*158delinsAAT	ENSP00000433191.1:n.*156_*158delinsAAT
ENST00000527953.5:n.1593_1595delinsAAT
ENST00000531714.1:n.487_489delinsAAT
ENST00000533320.5:n.1533_1535delinsAAT
ENST00000535898.5:c.993_995delinsAAT	ENSP00000445062.1:p.Arg331=
ENST00000539050.5:c.1089_1091delinsAAT	ENSP00000442343.2:p.Arg363=
ENST00000623108.3:c.1089_1091delinsAAT	ENSP00000485110.1:p.Arg363=
NM_000770.3:c.1299_1301delinsAAT MANE Select	NP_000761.3:p.Arg433=
NM_001198853.1:c.1089_1091delinsAAT	NP_001185782.1:p.Arg363=
NM_001198854.1:c.993_995delinsAAT	NP_001185783.1:p.Arg331=
NM_001198855.1:c.1089_1091delinsAAT	NP_001185784.1:p.Arg363=
XR_945610.1:n.1434_1436delinsAAT