Canonical Allele Identifier: CA1929278381

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850157_94850159delinsCTT , CM000672.2:g.94850157_94850159delinsCTT	GRCh38
NC_000010.10:g.96609914_96609916delinsCTT , CM000672.1:g.96609914_96609916delinsCTT	GRCh37
NC_000010.9:g.96599904_96599906delinsCTT	NCBI36
NG_008384.2:g.92452_92454delinsCTT
NG_008384.3:g.92477_92479delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+99_1291+101delinsCTT MANE Select	ENSP00000360372.3:n.1291+99_1291+101delinsCTT
ENST00000645461.1:n.2202+99_2202+101delinsCTT
ENST00000371321.7:c.1291+99_1291+101delinsCTT	ENSP00000360372.3:n.1291+99_1291+101delinsCTT
ENST00000464755.1:c.2054+99_2054+101delinsCTT	ENSP00000483243.1:n.2054+99_2054+101delinsCTT
NM_000769.2:c.1291+99_1291+101delinsCTT	NP_000760.1:n.1291+99_1291+101delinsCTT
NM_000769.4:c.1291+99_1291+101delinsCTT MANE Select	NP_000760.1:n.1291+99_1291+101delinsCTT