Canonical Allele Identifier: CA1929279768

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852532_94852540delinsCCATCCATT , CM000672.2:g.94852532_94852540delinsCCATCCATT	GRCh38
NC_000010.10:g.96612289_96612297delinsCCATCCATT , CM000672.1:g.96612289_96612297delinsCCATCCATT	GRCh37
NC_000010.9:g.96602279_96602287delinsCCATCCATT	NCBI36
NG_008384.2:g.94827_94835delinsCCATCCATT
NG_008384.3:g.94852_94860delinsCCATCCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1292-201_1292-193delinsCCATCCATT MANE Select	ENSP00000360372.3:n.1292-201_1292-193delinsCCATCCATT
ENST00000645461.1:n.2203-201_2203-193delinsCCATCCATT
ENST00000371321.7:c.1292-201_1292-193delinsCCATCCATT	ENSP00000360372.3:n.1292-201_1292-193delinsCCATCCATT
ENST00000464755.1:c.2055-201_2055-193delinsCCATCCATT	ENSP00000483243.1:n.2055-201_2055-193delinsCCATCCATT
NM_000769.2:c.1292-201_1292-193delinsCCATCCATT	NP_000760.1:n.1292-201_1292-193delinsCCATCCATT
NM_000769.4:c.1292-201_1292-193delinsCCATCCATT MANE Select	NP_000760.1:n.1292-201_1292-193delinsCCATCCATT