Canonical Allele Identifier: CA1929218888

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775614_94775615delinsAG , CM000672.2:g.94775614_94775615delinsAG	GRCh38
NC_000010.10:g.96535371_96535372delinsAG , CM000672.1:g.96535371_96535372delinsAG	GRCh37
NC_000010.9:g.96525361_96525362delinsAG	NCBI36
NG_008384.2:g.17909_17910delinsAG
NG_008384.3:g.17934_17935delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+75_481+76delinsAG MANE Select	ENSP00000360372.3:n.481+75_481+76delinsAG
ENST00000645461.1:n.1534+75_1534+76delinsAG
ENST00000371321.7:c.481+75_481+76delinsAG	ENSP00000360372.3:n.481+75_481+76delinsAG
ENST00000464755.1:c.1244+75_1244+76delinsAG	ENSP00000483243.1:n.1244+75_1244+76delinsAG
ENST00000480405.2:c.*67_*68delinsAG	ENSP00000483847.1:n.*67_*68delinsAG
NM_000769.2:c.481+75_481+76delinsAG	NP_000760.1:n.481+75_481+76delinsAG
NM_000769.4:c.481+75_481+76delinsAG MANE Select	NP_000760.1:n.481+75_481+76delinsAG