Canonical Allele Identifier: CA1929278453

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850257_94850258delinsTC , CM000672.2:g.94850257_94850258delinsTC	GRCh38
NC_000010.10:g.96610014_96610015delinsTC , CM000672.1:g.96610014_96610015delinsTC	GRCh37
NC_000010.9:g.96600004_96600005delinsTC	NCBI36
NG_008384.2:g.92552_92553delinsTC
NG_008384.3:g.92577_92578delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+199_1291+200delinsTC MANE Select	ENSP00000360372.3:n.1291+199_1291+200delinsTC
ENST00000645461.1:n.2202+199_2202+200delinsTC
ENST00000371321.7:c.1291+199_1291+200delinsTC	ENSP00000360372.3:n.1291+199_1291+200delinsTC
ENST00000464755.1:c.2054+199_2054+200delinsTC	ENSP00000483243.1:n.2054+199_2054+200delinsTC
NM_000769.2:c.1291+199_1291+200delinsTC	NP_000760.1:n.1291+199_1291+200delinsTC
NM_000769.4:c.1291+199_1291+200delinsTC MANE Select	NP_000760.1:n.1291+199_1291+200delinsTC