Canonical Allele Identifier: CA1929221725

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780800_94780801delinsGA , CM000672.2:g.94780800_94780801delinsGA	GRCh38
NC_000010.10:g.96540557_96540558delinsGA , CM000672.1:g.96540557_96540558delinsGA	GRCh37
NC_000010.9:g.96530547_96530548delinsGA	NCBI36
NG_008384.2:g.23095_23096delinsGA
NG_008384.3:g.23120_23121delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.642+141_642+142delinsGA MANE Select	ENSP00000360372.3:n.642+141_642+142delinsGA
ENST00000645461.1:n.1695+141_1695+142delinsGA
ENST00000371321.7:c.642+141_642+142delinsGA	ENSP00000360372.3:n.642+141_642+142delinsGA
ENST00000464755.1:c.1405+141_1405+142delinsGA	ENSP00000483243.1:n.1405+141_1405+142delinsGA
NM_000769.2:c.642+141_642+142delinsGA	NP_000760.1:n.642+141_642+142delinsGA
NM_000769.4:c.642+141_642+142delinsGA MANE Select	NP_000760.1:n.642+141_642+142delinsGA