Canonical Allele Identifier: CA1929359548

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95041237_95041238delinsAT , CM000672.2:g.95041237_95041238delinsAT	GRCh38
NC_000010.10:g.96800994_96800995delinsAT , CM000672.1:g.96800994_96800995delinsAT	GRCh37
NC_000010.9:g.96790984_96790985delinsAT	NCBI36
NG_007972.1:g.33260_33261delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1149+1652_1149+1653delinsAT MANE Select	ENSP00000360317.3:n.1149+1652_1149+1653delinsAT
ENST00000371270.5:c.1149+1652_1149+1653delinsAT	ENSP00000360317.3:n.1149+1652_1149+1653delinsAT
ENST00000479946.2:n.1454-278_1454-277delinsAT
ENST00000490994.6:c.*935+1652_*935+1653delinsAT	ENSP00000433314.1:n.*935+1652_*935+1653delinsAT
ENST00000525991.5:c.*724+1652_*724+1653delinsAT	ENSP00000433842.1:n.*724+1652_*724+1653delinsAT
ENST00000526814.5:n.1404+1652_1404+1653delinsAT
ENST00000527420.5:c.1150-278_1150-277delinsAT	ENSP00000433191.1:n.1150-278_1150-277delinsAT
ENST00000527953.5:n.1405-278_1405-277delinsAT
ENST00000533320.5:n.1383+1652_1383+1653delinsAT
ENST00000535898.5:c.843+1652_843+1653delinsAT	ENSP00000445062.1:n.843+1652_843+1653delinsAT
ENST00000539050.5:c.939+1652_939+1653delinsAT	ENSP00000442343.2:n.939+1652_939+1653delinsAT
ENST00000623108.3:c.939+1652_939+1653delinsAT	ENSP00000485110.1:n.939+1652_939+1653delinsAT
ENST00000628935.1:c.892-278_892-277delinsAT	ENSP00000487145.1:n.892-278_892-277delinsAT
NM_000770.3:c.1149+1652_1149+1653delinsAT MANE Select	NP_000761.3:n.1149+1652_1149+1653delinsAT
NM_001198853.1:c.939+1652_939+1653delinsAT	NP_001185782.1:n.939+1652_939+1653delinsAT
NM_001198854.1:c.843+1652_843+1653delinsAT	NP_001185783.1:n.843+1652_843+1653delinsAT
NM_001198855.1:c.939+1652_939+1653delinsAT	NP_001185784.1:n.939+1652_939+1653delinsAT
XR_945610.1:n.1246-278_1246-277delinsAT