Canonical Allele Identifier: CA1929375265

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037187_95037188delinsCT , CM000672.2:g.95037187_95037188delinsCT	GRCh38
NC_000010.10:g.96796944_96796945delinsCT , CM000672.1:g.96796944_96796945delinsCT	GRCh37
NC_000010.9:g.96786934_96786935delinsCT	NCBI36
NG_007972.1:g.37310_37311delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1413_1414delinsAG MANE Select	ENSP00000360317.3:p.Ala471=
ENST00000371270.5:c.1413_1414delinsAG	ENSP00000360317.3:p.Ala471=
ENST00000490994.6:c.*1199_*1200delinsAG	ENSP00000433314.1:n.*1199_*1200delinsAG
ENST00000525991.5:c.*988_*989delinsAG	ENSP00000433842.1:n.*988_*989delinsAG
ENST00000526814.5:n.1668_1669delinsAG
ENST00000527420.5:c.*270_*271delinsAG	ENSP00000433191.1:n.*270_*271delinsAG
ENST00000527953.5:n.1707_1708delinsAG
ENST00000531714.1:n.601_602delinsAG
ENST00000533320.5:n.1647_1648delinsAG
ENST00000535898.5:c.1107_1108delinsAG	ENSP00000445062.1:p.Ala369=
ENST00000539050.5:c.1203_1204delinsAG	ENSP00000442343.2:p.Ala401=
ENST00000623108.3:c.1203_1204delinsAG	ENSP00000485110.1:p.Ala401=
NM_000770.3:c.1413_1414delinsAG MANE Select	NP_000761.3:p.Ala471=
NM_001198853.1:c.1203_1204delinsAG	NP_001185782.1:p.Ala401=
NM_001198854.1:c.1107_1108delinsAG	NP_001185783.1:p.Ala369=
NM_001198855.1:c.1203_1204delinsAG	NP_001185784.1:p.Ala401=
XR_945610.1:n.1548_1549delinsAG