Canonical Allele Identifier: CA1929221492
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780366_94780367delinsCT , CM000672.2:g.94780366_94780367delinsCT GRCh38
NC_000010.10:g.96540123_96540124delinsCT , CM000672.1:g.96540123_96540124delinsCT GRCh37
NC_000010.9:g.96530113_96530114delinsCT NCBI36
NG_008384.2:g.22661_22662delinsCT
NG_008384.3:g.22686_22687delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-133_482-132delinsCT MANE Select ENSP00000360372.3:n.482-133_482-132delins...
ENST00000645461.1:n.1535-133_1535-132delinsCT
ENST00000371321.7:c.482-133_482-132delinsCT ENSP00000360372.3:n.482-133_482-132delins...
ENST00000464755.1:c.1245-133_1245-132delinsCT ENSP00000483243.1:n.1245-133_1245-132deli...
NM_000769.2:c.482-133_482-132delinsCT NP_000760.1:n.482-133_482-132delinsCT
NM_000769.4:c.482-133_482-132delinsCT MANE Select NP_000760.1:n.482-133_482-132delinsCT