Canonical Allele Identifier: CA2574628639

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94850005-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850007del , CM000672.2:g.94850007del	GRCh38
NC_000010.10:g.96609764del , CM000672.1:g.96609764del	GRCh37
NC_000010.9:g.96599754del	NCBI36
NG_008384.2:g.92302del
NG_008384.3:g.92327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1240del MANE Select	ENSP00000360372.3:p.Asp414MetfsTer?
ENST00000645461.1:n.2151del
ENST00000371321.7:c.1240del	ENSP00000360372.3:p.Asp414MetfsTer?
ENST00000464755.1:c.2003del	ENSP00000483243.1:n.2003del
NM_000769.2:c.1240del	NP_000760.1:p.Asp414MetfsTer?
NM_000769.4:c.1240del MANE Select	NP_000760.1:p.Asp414MetfsTer?