Canonical Allele Identifier: CA1929359383

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95041038_95041039delinsCA , CM000672.2:g.95041038_95041039delinsCA	GRCh38
NC_000010.10:g.96800795_96800796delinsCA , CM000672.1:g.96800795_96800796delinsCA	GRCh37
NC_000010.9:g.96790785_96790786delinsCA	NCBI36
NG_007972.1:g.33459_33460delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1149+1851_1149+1852delinsTG MANE Select	ENSP00000360317.3:n.1149+1851_1149+1852de...
ENST00000371270.5:c.1149+1851_1149+1852delinsTG	ENSP00000360317.3:n.1149+1851_1149+1852de...
ENST00000479946.2:n.1454-79_1454-78delinsTG
ENST00000490994.6:c.*935+1851_*935+1852delinsTG	ENSP00000433314.1:n.*935+1851_*935+1852de...
ENST00000525991.5:c.*724+1851_*724+1852delinsTG	ENSP00000433842.1:n.*724+1851_*724+1852de...
ENST00000526814.5:n.1404+1851_1404+1852delinsTG
ENST00000527420.5:c.1150-79_1150-78delinsTG	ENSP00000433191.1:n.1150-79_1150-78delins...
ENST00000527953.5:n.1405-79_1405-78delinsTG
ENST00000533320.5:n.1383+1851_1383+1852delinsTG
ENST00000535898.5:c.843+1851_843+1852delinsTG	ENSP00000445062.1:n.843+1851_843+1852deli...
ENST00000539050.5:c.939+1851_939+1852delinsTG	ENSP00000442343.2:n.939+1851_939+1852deli...
ENST00000623108.3:c.939+1851_939+1852delinsTG	ENSP00000485110.1:n.939+1851_939+1852deli...
ENST00000628935.1:c.892-79_892-78delinsTG	ENSP00000487145.1:n.892-79_892-78delinsTG...
NM_000770.3:c.1149+1851_1149+1852delinsTG MANE Select	NP_000761.3:n.1149+1851_1149+1852delinsTG...
NM_001198853.1:c.939+1851_939+1852delinsTG	NP_001185782.1:n.939+1851_939+1852delinsT...
NM_001198854.1:c.843+1851_843+1852delinsTG	NP_001185783.1:n.843+1851_843+1852delinsT...
NM_001198855.1:c.939+1851_939+1852delinsTG	NP_001185784.1:n.939+1851_939+1852delinsT...
XR_945610.1:n.1246-79_1246-78delinsTG