Canonical Allele Identifier: CA1929213579

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762685_94762688delinsTAAC , CM000672.2:g.94762685_94762688delinsTAAC	GRCh38
NC_000010.10:g.96522442_96522445delinsTAAC , CM000672.1:g.96522442_96522445delinsTAAC	GRCh37
NC_000010.9:g.96512432_96512435delinsTAAC	NCBI36
NG_008384.2:g.4980_4983delinsTAAC
NG_008384.3:g.5005_5008delinsTAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.-21_-18delinsTAAC MANE Select	ENSP00000360372.3:n.-21_-18delinsTAAC
ENST00000371321.7:c.-21_-18delinsTAAC	ENSP00000360372.3:n.-21_-18delinsTAAC
ENST00000464755.1:c.932-12373_932-12370delinsTAAC	ENSP00000483243.1:n.932-12373_932-12370delinsTAAC
ENST00000480405.2:c.-21_-18delinsTAAC	ENSP00000483847.1:n.-21_-18delinsTAAC
NM_000769.2:c.-21_-18delinsTAAC	NP_000760.1:n.-21_-18delinsTAAC
NM_000769.4:c.-21_-18delinsTAAC MANE Select	NP_000760.1:n.-21_-18delinsTAAC