Canonical Allele Identifier: CA2695212478
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762712_94762715delinsTCTC , CM000672.2:g.94762712_94762715delinsTCTC GRCh38
NC_000010.10:g.96522469_96522472delinsTCTC , CM000672.1:g.96522469_96522472delinsTCTC GRCh37
NC_000010.9:g.96512459_96512462delinsTCTC NCBI36
NG_008384.2:g.5007_5010delinsTCTC
NG_008384.3:g.5032_5035delinsTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.7_10delinsTCTC MANE Select ENSP00000360372.3:p.Pro3_Phe4delinsSerLeu...
ENST00000371321.7:c.7_10delinsTCTC ENSP00000360372.3:p.Pro3_Phe4delinsSerLeu...
ENST00000464755.1:c.932-12346_932-12343delinsTCTC ENSP00000483243.1:n.932-12346_932-12343de...
ENST00000480405.2:c.7_10delinsTCTC ENSP00000483847.1:p.Pro3_Phe4delinsSerLeu...
NM_000769.2:c.7_10delinsTCTC NP_000760.1:p.Pro3_Phe4delinsSerLeu
NM_000769.4:c.7_10delinsTCTC MANE Select NP_000760.1:p.Pro3_Phe4delinsSerLeu