Canonical Allele Identifier: CA2512277449
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852590_94852594del , CM000672.2:g.94852590_94852594del GRCh38
NC_000010.10:g.96612347_96612351del , CM000672.1:g.96612347_96612351del GRCh37
NC_000010.9:g.96602337_96602341del NCBI36
NG_008384.2:g.94885_94889del
NG_008384.3:g.94910_94914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-143_1292-139del MANE Select ENSP00000360372.3:n.1292-143_1292-139del
ENST00000645461.1:n.2203-143_2203-139del
ENST00000371321.7:c.1292-143_1292-139del ENSP00000360372.3:n.1292-143_1292-139del
ENST00000464755.1:c.2055-143_2055-139del ENSP00000483243.1:n.2055-143_2055-139del
NM_000769.2:c.1292-143_1292-139del NP_000760.1:n.1292-143_1292-139del
NM_000769.4:c.1292-143_1292-139del MANE Select NP_000760.1:n.1292-143_1292-139del