Canonical Allele Identifier: CA1929374902

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037005_95037006delinsTG , CM000672.2:g.95037005_95037006delinsTG	GRCh38
NC_000010.10:g.96796762_96796763delinsTG , CM000672.1:g.96796762_96796763delinsTG	GRCh37
NC_000010.9:g.96786752_96786753delinsTG	NCBI36
NG_007972.1:g.37492_37493delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*122_*123delinsCA MANE Select	ENSP00000360317.3:n.*122_*123delinsCA
ENST00000371270.5:c.*122_*123delinsCA	ENSP00000360317.3:n.*122_*123delinsCA
ENST00000490994.6:c.*1381_*1382delinsCA	ENSP00000433314.1:n.*1381_*1382delinsCA
ENST00000525991.5:c.*1170_*1171delinsCA	ENSP00000433842.1:n.*1170_*1171delinsCA
ENST00000526814.5:n.1850_1851delinsCA
ENST00000527420.5:c.*452_*453delinsCA	ENSP00000433191.1:n.*452_*453delinsCA
ENST00000527953.5:n.1889_1890delinsCA
ENST00000533320.5:n.1829_1830delinsCA
ENST00000535898.5:c.*122_*123delinsCA	ENSP00000445062.1:n.*122_*123delinsCA
ENST00000539050.5:c.*122_*123delinsCA	ENSP00000442343.2:n.*122_*123delinsCA
ENST00000623108.3:c.*122_*123delinsCA	ENSP00000485110.1:n.*122_*123delinsCA
NM_000770.3:c.*122_*123delinsCA MANE Select	NP_000761.3:n.*122_*123delinsCA
NM_001198853.1:c.*122_*123delinsCA	NP_001185782.1:n.*122_*123delinsCA
NM_001198854.1:c.*122_*123delinsCA	NP_001185783.1:n.*122_*123delinsCA
NM_001198855.1:c.*122_*123delinsCA	NP_001185784.1:n.*122_*123delinsCA