Canonical Allele Identifier: CA1929221714

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780785_94780786delinsTG , CM000672.2:g.94780785_94780786delinsTG	GRCh38
NC_000010.10:g.96540542_96540543delinsTG , CM000672.1:g.96540542_96540543delinsTG	GRCh37
NC_000010.9:g.96530532_96530533delinsTG	NCBI36
NG_008384.2:g.23080_23081delinsTG
NG_008384.3:g.23105_23106delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.642+126_642+127delinsTG MANE Select	ENSP00000360372.3:n.642+126_642+127delinsTG
ENST00000645461.1:n.1695+126_1695+127delinsTG
ENST00000371321.7:c.642+126_642+127delinsTG	ENSP00000360372.3:n.642+126_642+127delinsTG
ENST00000464755.1:c.1405+126_1405+127delinsTG	ENSP00000483243.1:n.1405+126_1405+127delinsTG
NM_000769.2:c.642+126_642+127delinsTG	NP_000760.1:n.642+126_642+127delinsTG
NM_000769.4:c.642+126_642+127delinsTG MANE Select	NP_000760.1:n.642+126_642+127delinsTG