Canonical Allele Identifier: CA2789064542

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780722_94780723insCACACCCAACAC , CM000672.2:g.94780722_94780723insCACACCCAACAC	GRCh38
NC_000010.10:g.96540479_96540480insCACACCCAACAC , CM000672.1:g.96540479_96540480insCACACCCAACAC	GRCh37
NC_000010.9:g.96530469_96530470insCACACCCAACAC	NCBI36
NG_008384.2:g.23017_23018insCACACCCAACAC
NG_008384.3:g.23042_23043insCACACCCAACAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.642+63_642+64insCACACCCAACAC MANE Select	ENSP00000360372.3:n.642+63_642+64insCACACCCAACAC
ENST00000645461.1:n.1695+63_1695+64insCACACCCAACAC
ENST00000371321.7:c.642+63_642+64insCACACCCAACAC	ENSP00000360372.3:n.642+63_642+64insCACACCCAACAC
ENST00000464755.1:c.1405+63_1405+64insCACACCCAACAC	ENSP00000483243.1:n.1405+63_1405+64insCACACCCAACAC
NM_000769.2:c.642+63_642+64insCACACCCAACAC	NP_000760.1:n.642+63_642+64insCACACCCAACAC
NM_000769.4:c.642+63_642+64insCACACCCAACAC MANE Select	NP_000760.1:n.642+63_642+64insCACACCCAACAC