Canonical Allele Identifier: CA2610271169

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95067195-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067198_95067199del , CM000672.2:g.95067198_95067199del	GRCh38
NC_000010.10:g.96826955_96826956del , CM000672.1:g.96826955_96826956del	GRCh37
NC_000010.9:g.96816945_96816946del	NCBI36
NG_007972.1:g.7301_7302del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.481+11_481+12del MANE Select	ENSP00000360317.3:n.481+11_481+12del
ENST00000371270.5:c.481+11_481+12del	ENSP00000360317.3:n.481+11_481+12del
ENST00000479946.2:n.785+11_785+12del
ENST00000490994.6:c.*267+11_*267+12del	ENSP00000433314.1:n.*267+11_*267+12del
ENST00000525991.5:c.*56+11_*56+12del	ENSP00000433842.1:n.*56+11_*56+12del
ENST00000526814.5:n.736+11_736+12del
ENST00000527420.5:c.481+11_481+12del	ENSP00000433191.1:n.481+11_481+12del
ENST00000527953.5:n.736+11_736+12del
ENST00000533320.5:n.715+11_715+12del
ENST00000535898.5:c.175+11_175+12del	ENSP00000445062.1:n.175+11_175+12del
ENST00000539050.5:c.271+11_271+12del	ENSP00000442343.2:n.271+11_271+12del
ENST00000623108.3:c.271+11_271+12del	ENSP00000485110.1:n.271+11_271+12del
ENST00000628935.1:c.223+11_223+12del	ENSP00000487145.1:n.223+11_223+12del
NM_000770.3:c.481+11_481+12del MANE Select	NP_000761.3:n.481+11_481+12del
NM_001198853.1:c.271+11_271+12del	NP_001185782.1:n.271+11_271+12del
NM_001198854.1:c.175+11_175+12del	NP_001185783.1:n.175+11_175+12del
NM_001198855.1:c.271+11_271+12del	NP_001185784.1:n.271+11_271+12del
XR_945610.1:n.577+11_577+12del