Canonical Allele Identifier: CA931394262

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95049268_95049269del , CM000672.2:g.95049268_95049269del	GRCh38
NC_000010.10:g.96809025_96809026del , CM000672.1:g.96809025_96809026del	GRCh37
NC_000010.9:g.96799015_96799016del	NCBI36
NG_007972.1:g.25229_25230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.820-3318_820-3317del MANE Select	ENSP00000360317.3:n.820-3318_820-3317del
ENST00000371270.5:c.820-3318_820-3317del	ENSP00000360317.3:n.820-3318_820-3317del
ENST00000479946.2:n.1124-3318_1124-3317del
ENST00000490994.6:c.*606-3318_*606-3317del	ENSP00000433314.1:n.*606-3318_*606-3317del
ENST00000525991.5:c.*395-3318_*395-3317del	ENSP00000433842.1:n.*395-3318_*395-3317del
ENST00000526814.5:n.1075-3318_1075-3317del
ENST00000527420.5:c.820-3318_820-3317del	ENSP00000433191.1:n.820-3318_820-3317del
ENST00000527953.5:n.1075-3318_1075-3317del
ENST00000533320.5:n.1054-3318_1054-3317del
ENST00000535898.5:c.514-3318_514-3317del	ENSP00000445062.1:n.514-3318_514-3317del
ENST00000539050.5:c.610-3318_610-3317del	ENSP00000442343.2:n.610-3318_610-3317del
ENST00000623108.3:c.610-3318_610-3317del	ENSP00000485110.1:n.610-3318_610-3317del
ENST00000628935.1:c.562-3318_562-3317del	ENSP00000487145.1:n.562-3318_562-3317del
NM_000770.3:c.820-3318_820-3317del MANE Select	NP_000761.3:n.820-3318_820-3317del
NM_001198853.1:c.610-3318_610-3317del	NP_001185782.1:n.610-3318_610-3317del
NM_001198854.1:c.514-3318_514-3317del	NP_001185783.1:n.514-3318_514-3317del
NM_001198855.1:c.610-3318_610-3317del	NP_001185784.1:n.610-3318_610-3317del
XR_945610.1:n.916-3318_916-3317del