Canonical Allele Identifier: CA2512274413
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852474_94852475insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC , CM000672.2:g.94852474_94852475insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC GRCh38
NC_000010.10:g.96612231_96612232insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC , CM000672.1:g.96612231_96612232insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC GRCh37
NC_000010.9:g.96602221_96602222insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC NCBI36
NG_008384.2:g.94769_94770insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC
NG_008384.3:g.94794_94795insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC MANE Select ENSP00000360372.3:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGG...
ENST00000645461.1:n.2203-259_2203-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC
ENST00000371321.7:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC ENSP00000360372.3:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGG...
ENST00000464755.1:c.2055-259_2055-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC ENSP00000483243.1:n.2055-259_2055-258insCAATGCTTTCCGAGTCCAAGG...
NM_000769.2:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC NP_000760.1:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATT...
NM_000769.4:c.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATTCCCTCACCATGACCGAGCTGGCAATTACTACCAATACCCTCCCGGCACGCCTCTCCCGCGTTGTGGCACGCCTGGAGAAGGACGGCTACGTCCGCCGTTCCCTC MANE Select NP_000760.1:n.1292-259_1292-258insCAATGCTTTCCGAGTCCAAGGATCATT...