Canonical Allele Identifier: CA1929213964

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762885_94762888delinsCCTT , CM000672.2:g.94762885_94762888delinsCCTT	GRCh38
NC_000010.10:g.96522642_96522645delinsCCTT , CM000672.1:g.96522642_96522645delinsCCTT	GRCh37
NC_000010.9:g.96512632_96512635delinsCCTT	NCBI36
NG_008384.2:g.5180_5183delinsCCTT
NG_008384.3:g.5205_5208delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.168+12_168+15delinsCCTT MANE Select	ENSP00000360372.3:n.168+12_168+15delinsCCTT
ENST00000371321.7:c.168+12_168+15delinsCCTT	ENSP00000360372.3:n.168+12_168+15delinsCCTT
ENST00000464755.1:c.932-12173_932-12170delinsCCTT	ENSP00000483243.1:n.932-12173_932-12170delinsCCTT
ENST00000480405.2:c.168+12_168+15delinsCCTT	ENSP00000483847.1:n.168+12_168+15delinsCCTT
NM_000769.2:c.168+12_168+15delinsCCTT	NP_000760.1:n.168+12_168+15delinsCCTT
NM_000769.4:c.168+12_168+15delinsCCTT MANE Select	NP_000760.1:n.168+12_168+15delinsCCTT