Canonical Allele Identifier: CA1929222401
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781858_94781859delinsCG , CM000672.2:g.94781858_94781859delinsCG GRCh38
NC_000010.10:g.96541615_96541616delinsCG , CM000672.1:g.96541615_96541616delinsCG GRCh37
NC_000010.9:g.96531605_96531606delinsCG NCBI36
NG_008384.2:g.24153_24154delinsCG
NG_008384.3:g.24178_24179delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.680_681delinsCG MANE Select ENSP00000360372.3:p.Pro227=
ENST00000645461.1:n.1733_1734delinsCG
ENST00000371321.7:c.680_681delinsCG ENSP00000360372.3:p.Pro227=
ENST00000464755.1:c.1443_1444delinsCG ENSP00000483243.1:n.1443_1444delinsCG
NM_000769.2:c.680_681delinsCG NP_000760.1:p.Pro227=
NM_000769.4:c.680_681delinsCG MANE Select NP_000760.1:p.Pro227=