Canonical Allele Identifier: CA1929214414

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94763313_94763314delinsGC , CM000672.2:g.94763313_94763314delinsGC	GRCh38
NC_000010.10:g.96523070_96523071delinsGC , CM000672.1:g.96523070_96523071delinsGC	GRCh37
NC_000010.9:g.96513060_96513061delinsGC	NCBI36
NG_008384.2:g.5608_5609delinsGC
NG_008384.3:g.5633_5634delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.168+440_168+441delinsGC MANE Select	ENSP00000360372.3:n.168+440_168+441delinsGC
ENST00000371321.7:c.168+440_168+441delinsGC	ENSP00000360372.3:n.168+440_168+441delinsGC
ENST00000464755.1:c.932-11745_932-11744delinsGC	ENSP00000483243.1:n.932-11745_932-11744delinsGC
ENST00000480405.2:c.168+440_168+441delinsGC	ENSP00000483847.1:n.168+440_168+441delinsGC
NM_000769.2:c.168+440_168+441delinsGC	NP_000760.1:n.168+440_168+441delinsGC
NM_000769.4:c.168+440_168+441delinsGC MANE Select	NP_000760.1:n.168+440_168+441delinsGC