Canonical Allele Identifier: CA1929218987

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775781_94775782delinsCT , CM000672.2:g.94775781_94775782delinsCT	GRCh38
NC_000010.10:g.96535538_96535539delinsCT , CM000672.1:g.96535538_96535539delinsCT	GRCh37
NC_000010.9:g.96525528_96525529delinsCT	NCBI36
NG_008384.2:g.18076_18077delinsCT
NG_008384.3:g.18101_18102delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+242_481+243delinsCT MANE Select	ENSP00000360372.3:n.481+242_481+243delinsCT
ENST00000645461.1:n.1534+242_1534+243delinsCT
ENST00000371321.7:c.481+242_481+243delinsCT	ENSP00000360372.3:n.481+242_481+243delinsCT
ENST00000464755.1:c.1244+242_1244+243delinsCT	ENSP00000483243.1:n.1244+242_1244+243delinsCT
ENST00000480405.2:c.*234_*235delinsCT	ENSP00000483847.1:n.*234_*235delinsCT
NM_000769.2:c.481+242_481+243delinsCT	NP_000760.1:n.481+242_481+243delinsCT
NM_000769.4:c.481+242_481+243delinsCT MANE Select	NP_000760.1:n.481+242_481+243delinsCT