Canonical Allele Identifier: CA2504449400
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780444_94780445insGTAAAC , CM000672.2:g.94780444_94780445insGTAAAC GRCh38
NC_000010.10:g.96540201_96540202insGTAAAC , CM000672.1:g.96540201_96540202insGTAAAC GRCh37
NC_000010.9:g.96530191_96530192insGTAAAC NCBI36
NG_008384.2:g.22739_22740insGTAAAC
NG_008384.3:g.22764_22765insGTAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.482-55_482-54insGTAAAC MANE Select ENSP00000360372.3:n.482-55_482-54insGTAAAC
ENST00000645461.1:n.1535-55_1535-54insGTAAAC
ENST00000371321.7:c.482-55_482-54insGTAAAC ENSP00000360372.3:n.482-55_482-54insGTAAAC
ENST00000464755.1:c.1245-55_1245-54insGTAAAC ENSP00000483243.1:n.1245-55_1245-54insGTAAAC
NM_000769.2:c.482-55_482-54insGTAAAC NP_000760.1:n.482-55_482-54insGTAAAC
NM_000769.4:c.482-55_482-54insGTAAAC MANE Select NP_000760.1:n.482-55_482-54insGTAAAC