Canonical Allele Identifier: CA1929218623
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775182_94775184delinsGCC , CM000672.2:g.94775182_94775184delinsGCC GRCh38
NC_000010.10:g.96534939_96534941delinsGCC , CM000672.1:g.96534939_96534941delinsGCC GRCh37
NC_000010.9:g.96524929_96524931delinsGCC NCBI36
NG_008384.2:g.17477_17479delinsGCC
NG_008384.3:g.17502_17504delinsGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.293_295delinsGCC MANE Select ENSP00000360372.3:p.Gly98=
ENST00000645461.1:n.1346_1348delinsGCC
ENST00000371321.7:c.293_295delinsGCC ENSP00000360372.3:p.Gly98=
ENST00000464755.1:c.1056_1058delinsGCC ENSP00000483243.1:n.1056_1058delinsGCC
ENST00000480405.2:c.293_295delinsGCC ENSP00000483847.1:p.Gly98=
NM_000769.2:c.293_295delinsGCC NP_000760.1:p.Gly98=
NM_000769.4:c.293_295delinsGCC MANE Select NP_000760.1:p.Gly98=