Canonical Allele Identifier: CA2610263785

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94775210-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775213_94775214del , CM000672.2:g.94775213_94775214del	GRCh38
NC_000010.10:g.96534970_96534971del , CM000672.1:g.96534970_96534971del	GRCh37
NC_000010.9:g.96524960_96524961del	NCBI36
NG_008384.2:g.17508_17509del
NG_008384.3:g.17533_17534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.324_325del MANE Select	ENSP00000360372.3:p.Gly109IlefsTer?
ENST00000645461.1:n.1377_1378del
ENST00000371321.7:c.324_325del	ENSP00000360372.3:p.Gly109IlefsTer?
ENST00000464755.1:c.1087_1088del	ENSP00000483243.1:n.1087_1088del
ENST00000480405.2:c.324_325del	ENSP00000483847.1:p.Gly109IlefsTer?
NM_000769.2:c.324_325del	NP_000760.1:p.Gly109IlefsTer?
NM_000769.4:c.324_325del MANE Select	NP_000760.1:p.Gly109IlefsTer?