Canonical Allele Identifier: CA2610271170

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95067269-GCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067273_95067275del , CM000672.2:g.95067273_95067275del	GRCh38
NC_000010.10:g.96827030_96827032del , CM000672.1:g.96827030_96827032del	GRCh37
NC_000010.9:g.96817020_96817022del	NCBI36
NG_007972.1:g.7226_7228del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.417_419del MANE Select	ENSP00000360317.3:p.Arg139del
ENST00000371270.5:c.417_419del	ENSP00000360317.3:p.Arg139del
ENST00000479946.2:n.721_723del
ENST00000490994.6:c.*203_*205del	ENSP00000433314.1:n.*203_*205del
ENST00000525991.5:c.292_294del	ENSP00000433842.1:p.Glu98del
ENST00000526814.5:n.672_674del
ENST00000527420.5:c.417_419del	ENSP00000433191.1:p.Arg139del
ENST00000527953.5:n.672_674del
ENST00000533320.5:n.651_653del
ENST00000535898.5:c.111_113del	ENSP00000445062.1:p.Arg37del
ENST00000539050.5:c.207_209del	ENSP00000442343.2:p.Arg69del
ENST00000623108.3:c.207_209del	ENSP00000485110.1:p.Arg69del
ENST00000628935.1:c.159_161del	ENSP00000487145.1:p.Arg53del
NM_000770.3:c.417_419del MANE Select	NP_000761.3:p.Arg139del
NM_001198853.1:c.207_209del	NP_001185782.1:p.Arg69del
NM_001198854.1:c.111_113del	NP_001185783.1:p.Arg37del
NM_001198855.1:c.207_209del	NP_001185784.1:p.Arg69del
XR_945610.1:n.513_515del