Canonical Allele Identifier: CA1929218841

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775541_94775542delinsTG , CM000672.2:g.94775541_94775542delinsTG	GRCh38
NC_000010.10:g.96535298_96535299delinsTG , CM000672.1:g.96535298_96535299delinsTG	GRCh37
NC_000010.9:g.96525288_96525289delinsTG	NCBI36
NG_008384.2:g.17836_17837delinsTG
NG_008384.3:g.17861_17862delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+2_481+3delinsTG MANE Select	ENSP00000360372.3:n.481+2_481+3delinsTG
ENST00000645461.1:n.1534+2_1534+3delinsTG
ENST00000371321.7:c.481+2_481+3delinsTG	ENSP00000360372.3:n.481+2_481+3delinsTG
ENST00000464755.1:c.1244+2_1244+3delinsTG	ENSP00000483243.1:n.1244+2_1244+3delinsTG
ENST00000480405.2:c.483_484delinsTG	ENSP00000483847.1:p.Gly161=
NM_000769.2:c.481+2_481+3delinsTG	NP_000760.1:n.481+2_481+3delinsTG
NM_000769.4:c.481+2_481+3delinsTG MANE Select	NP_000760.1:n.481+2_481+3delinsTG