Canonical Allele Identifier: CA1929280017
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853027_94853028delinsTC , CM000672.2:g.94853027_94853028delinsTC GRCh38
NC_000010.10:g.96612784_96612785delinsTC , CM000672.1:g.96612784_96612785delinsTC GRCh37
NC_000010.9:g.96602774_96602775delinsTC NCBI36
NG_008384.2:g.95322_95323delinsTC
NG_008384.3:g.95347_95348delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*113_*114delinsTC MANE Select ENSP00000360372.3:n.*113_*114delinsTC
ENST00000645461.1:n.2497_2498delinsTC
ENST00000371321.7:c.*113_*114delinsTC ENSP00000360372.3:n.*113_*114delinsTC
ENST00000464755.1:c.2349_2350delinsTC ENSP00000483243.1:n.2349_2350delinsTC
NM_000769.2:c.*113_*114delinsTC NP_000760.1:n.*113_*114delinsTC
NM_000769.4:c.*113_*114delinsTC MANE Select NP_000760.1:n.*113_*114delinsTC