Canonical Allele Identifier: CA1929221667
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780695_94780697delinsTAC , CM000672.2:g.94780695_94780697delinsTAC GRCh38
NC_000010.10:g.96540452_96540454delinsTAC , CM000672.1:g.96540452_96540454delinsTAC GRCh37
NC_000010.9:g.96530442_96530444delinsTAC NCBI36
NG_008384.2:g.22990_22992delinsTAC
NG_008384.3:g.23015_23017delinsTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+36_642+38delinsTAC MANE Select ENSP00000360372.3:n.642+36_642+38delinsTA...
ENST00000645461.1:n.1695+36_1695+38delinsTAC
ENST00000371321.7:c.642+36_642+38delinsTAC ENSP00000360372.3:n.642+36_642+38delinsTA...
ENST00000464755.1:c.1405+36_1405+38delinsTAC ENSP00000483243.1:n.1405+36_1405+38delins...
NM_000769.2:c.642+36_642+38delinsTAC NP_000760.1:n.642+36_642+38delinsTAC
NM_000769.4:c.642+36_642+38delinsTAC MANE Select NP_000760.1:n.642+36_642+38delinsTAC