Canonical Allele Identifier: CA2610265113

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94850196-T-TACACC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850196_94850197insACACC , CM000672.2:g.94850196_94850197insACACC	GRCh38
NC_000010.10:g.96609953_96609954insACACC , CM000672.1:g.96609953_96609954insACACC	GRCh37
NC_000010.9:g.96599943_96599944insACACC	NCBI36
NG_008384.2:g.92491_92492insACACC
NG_008384.3:g.92516_92517insACACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+138_1291+139insACACC MANE Select	ENSP00000360372.3:n.1291+138_1291+139insACACC
ENST00000645461.1:n.2202+138_2202+139insACACC
ENST00000371321.7:c.1291+138_1291+139insACACC	ENSP00000360372.3:n.1291+138_1291+139insACACC
ENST00000464755.1:c.2054+138_2054+139insACACC	ENSP00000483243.1:n.2054+138_2054+139insACACC
NM_000769.2:c.1291+138_1291+139insACACC	NP_000760.1:n.1291+138_1291+139insACACC
NM_000769.4:c.1291+138_1291+139insACACC MANE Select	NP_000760.1:n.1291+138_1291+139insACACC