Canonical Allele Identifier: CA1929279787

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852558_94852559delinsAC , CM000672.2:g.94852558_94852559delinsAC	GRCh38
NC_000010.10:g.96612315_96612316delinsAC , CM000672.1:g.96612315_96612316delinsAC	GRCh37
NC_000010.9:g.96602305_96602306delinsAC	NCBI36
NG_008384.2:g.94853_94854delinsAC
NG_008384.3:g.94878_94879delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1292-175_1292-174delinsAC MANE Select	ENSP00000360372.3:n.1292-175_1292-174delinsAC
ENST00000645461.1:n.2203-175_2203-174delinsAC
ENST00000371321.7:c.1292-175_1292-174delinsAC	ENSP00000360372.3:n.1292-175_1292-174delinsAC
ENST00000464755.1:c.2055-175_2055-174delinsAC	ENSP00000483243.1:n.2055-175_2055-174delinsAC
NM_000769.2:c.1292-175_1292-174delinsAC	NP_000760.1:n.1292-175_1292-174delinsAC
NM_000769.4:c.1292-175_1292-174delinsAC MANE Select	NP_000760.1:n.1292-175_1292-174delinsAC