Canonical Allele Identifier: CA2610265074

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94850147-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850149_94850150del , CM000672.2:g.94850149_94850150del	GRCh38
NC_000010.10:g.96609906_96609907del , CM000672.1:g.96609906_96609907del	GRCh37
NC_000010.9:g.96599896_96599897del	NCBI36
NG_008384.2:g.92444_92445del
NG_008384.3:g.92469_92470del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+91_1291+92del MANE Select	ENSP00000360372.3:n.1291+91_1291+92del
ENST00000645461.1:n.2202+91_2202+92del
ENST00000371321.7:c.1291+91_1291+92del	ENSP00000360372.3:n.1291+91_1291+92del
ENST00000464755.1:c.2054+91_2054+92del	ENSP00000483243.1:n.2054+91_2054+92del
NM_000769.2:c.1291+91_1291+92del	NP_000760.1:n.1291+91_1291+92del
NM_000769.4:c.1291+91_1291+92del MANE Select	NP_000760.1:n.1291+91_1291+92del