Canonical Allele Identifier: CA1929359382

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95041038_95041040delinsCAG , CM000672.2:g.95041038_95041040delinsCAG	GRCh38
NC_000010.10:g.96800795_96800797delinsCAG , CM000672.1:g.96800795_96800797delinsCAG	GRCh37
NC_000010.9:g.96790785_96790787delinsCAG	NCBI36
NG_007972.1:g.33458_33460delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1149+1850_1149+1852delinsCTG MANE Select	ENSP00000360317.3:n.1149+1850_1149+1852de...
ENST00000371270.5:c.1149+1850_1149+1852delinsCTG	ENSP00000360317.3:n.1149+1850_1149+1852de...
ENST00000479946.2:n.1454-80_1454-78delinsCTG
ENST00000490994.6:c.*935+1850_*935+1852delinsCTG	ENSP00000433314.1:n.*935+1850_*935+1852de...
ENST00000525991.5:c.*724+1850_*724+1852delinsCTG	ENSP00000433842.1:n.*724+1850_*724+1852de...
ENST00000526814.5:n.1404+1850_1404+1852delinsCTG
ENST00000527420.5:c.1150-80_1150-78delinsCTG	ENSP00000433191.1:n.1150-80_1150-78delins...
ENST00000527953.5:n.1405-80_1405-78delinsCTG
ENST00000533320.5:n.1383+1850_1383+1852delinsCTG
ENST00000535898.5:c.843+1850_843+1852delinsCTG	ENSP00000445062.1:n.843+1850_843+1852deli...
ENST00000539050.5:c.939+1850_939+1852delinsCTG	ENSP00000442343.2:n.939+1850_939+1852deli...
ENST00000623108.3:c.939+1850_939+1852delinsCTG	ENSP00000485110.1:n.939+1850_939+1852deli...
ENST00000628935.1:c.892-80_892-78delinsCTG	ENSP00000487145.1:n.892-80_892-78delinsCT...
NM_000770.3:c.1149+1850_1149+1852delinsCTG MANE Select	NP_000761.3:n.1149+1850_1149+1852delinsCT...
NM_001198853.1:c.939+1850_939+1852delinsCTG	NP_001185782.1:n.939+1850_939+1852delinsC...
NM_001198854.1:c.843+1850_843+1852delinsCTG	NP_001185783.1:n.843+1850_843+1852delinsC...
NM_001198855.1:c.939+1850_939+1852delinsCTG	NP_001185784.1:n.939+1850_939+1852delinsC...
XR_945610.1:n.1246-80_1246-78delinsCTG