Canonical Allele Identifier: CA1929375021

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037088_95037089delinsCA , CM000672.2:g.95037088_95037089delinsCA	GRCh38
NC_000010.10:g.96796845_96796846delinsCA , CM000672.1:g.96796845_96796846delinsCA	GRCh37
NC_000010.9:g.96786835_96786836delinsCA	NCBI36
NG_007972.1:g.37409_37410delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*39_*40delinsTG MANE Select	ENSP00000360317.3:n.*39_*40delinsTG
ENST00000371270.5:c.*39_*40delinsTG	ENSP00000360317.3:n.*39_*40delinsTG
ENST00000490994.6:c.*1298_*1299delinsTG	ENSP00000433314.1:n.*1298_*1299delinsTG
ENST00000525991.5:c.*1087_*1088delinsTG	ENSP00000433842.1:n.*1087_*1088delinsTG
ENST00000526814.5:n.1767_1768delinsTG
ENST00000527420.5:c.*369_*370delinsTG	ENSP00000433191.1:n.*369_*370delinsTG
ENST00000527953.5:n.1806_1807delinsTG
ENST00000533320.5:n.1746_1747delinsTG
ENST00000535898.5:c.*39_*40delinsTG	ENSP00000445062.1:n.*39_*40delinsTG
ENST00000539050.5:c.*39_*40delinsTG	ENSP00000442343.2:n.*39_*40delinsTG
ENST00000623108.3:c.*39_*40delinsTG	ENSP00000485110.1:n.*39_*40delinsTG
NM_000770.3:c.*39_*40delinsTG MANE Select	NP_000761.3:n.*39_*40delinsTG
NM_001198853.1:c.*39_*40delinsTG	NP_001185782.1:n.*39_*40delinsTG
NM_001198854.1:c.*39_*40delinsTG	NP_001185783.1:n.*39_*40delinsTG
NM_001198855.1:c.*39_*40delinsTG	NP_001185784.1:n.*39_*40delinsTG