Canonical Allele Identifier: CA1929214412
Gene: CYP2C19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94763313_94763326delinsGCAGCTGTGGGTTT , CM000672.2:g.94763313_94763326delinsGCAGCTGTGGGTTT GRCh38
NC_000010.10:g.96523070_96523083delinsGCAGCTGTGGGTTT , CM000672.1:g.96523070_96523083delinsGCAGCTGTGGGTTT GRCh37
NC_000010.9:g.96513060_96513073delinsGCAGCTGTGGGTTT NCBI36
NG_008384.2:g.5608_5621delinsGCAGCTGTGGGTTT
NG_008384.3:g.5633_5646delinsGCAGCTGTGGGTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.168+440_168+453delinsGCAGCTGTGGGTTT MANE Select ENSP00000360372.3:n.168+440_168+453delins...
ENST00000371321.7:c.168+440_168+453delinsGCAGCTGTGGGTTT ENSP00000360372.3:n.168+440_168+453delins...
ENST00000464755.1:c.932-11745_932-11732delinsGCAGCTGTGGGTTT ENSP00000483243.1:n.932-11745_932-11732de...
ENST00000480405.2:c.168+440_168+453delinsGCAGCTGTGGGTTT ENSP00000483847.1:n.168+440_168+453delins...
NM_000769.2:c.168+440_168+453delinsGCAGCTGTGGGTTT NP_000760.1:n.168+440_168+453delinsGCAGCT...
NM_000769.4:c.168+440_168+453delinsGCAGCTGTGGGTTT MANE Select NP_000760.1:n.168+440_168+453delinsGCAGCT...
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