Canonical Allele Identifier: CA2501852120
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852585_94852586insGGCG , CM000672.2:g.94852585_94852586insGGCG GRCh38
NC_000010.10:g.96612342_96612343insGGCG , CM000672.1:g.96612342_96612343insGGCG GRCh37
NC_000010.9:g.96602332_96602333insGGCG NCBI36
NG_008384.2:g.94880_94881insGGCG
NG_008384.3:g.94905_94906insGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-148_1292-147insGGCG MANE Select ENSP00000360372.3:n.1292-148_1292-147insGGCG
ENST00000645461.1:n.2203-148_2203-147insGGCG
ENST00000371321.7:c.1292-148_1292-147insGGCG ENSP00000360372.3:n.1292-148_1292-147insGGCG
ENST00000464755.1:c.2055-148_2055-147insGGCG ENSP00000483243.1:n.2055-148_2055-147insGGCG
NM_000769.2:c.1292-148_1292-147insGGCG NP_000760.1:n.1292-148_1292-147insGGCG
NM_000769.4:c.1292-148_1292-147insGGCG MANE Select NP_000760.1:n.1292-148_1292-147insGGCG
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