Canonical Allele Identifier: CA2789068218

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94782288_94782289insTG , CM000672.2:g.94782288_94782289insTG	GRCh38
NC_000010.10:g.96542045_96542046insTG , CM000672.1:g.96542045_96542046insTG	GRCh37
NC_000010.9:g.96532035_96532036insTG	NCBI36
NG_008384.2:g.24583_24584insTG
NG_008384.3:g.24608_24609insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.819+291_819+292insTG MANE Select	ENSP00000360372.3:n.819+291_819+292insTG
ENST00000645461.1:n.1872+291_1872+292insTG
ENST00000371321.7:c.819+291_819+292insTG	ENSP00000360372.3:n.819+291_819+292insTG
ENST00000464755.1:c.1582+291_1582+292insTG	ENSP00000483243.1:n.1582+291_1582+292insTG
NM_000769.2:c.819+291_819+292insTG	NP_000760.1:n.819+291_819+292insTG
NM_000769.4:c.819+291_819+292insTG MANE Select	NP_000760.1:n.819+291_819+292insTG