Canonical Allele Identifier: CA2568394157

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775586del , CM000672.2:g.94775586del	GRCh38
NC_000010.10:g.96535343del , CM000672.1:g.96535343del	GRCh37
NC_000010.9:g.96525333del	NCBI36
NG_008384.2:g.17881del
NG_008384.3:g.17906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+47del MANE Select	ENSP00000360372.3:n.481+47del
ENST00000645461.1:n.1534+47del
ENST00000371321.7:c.481+47del	ENSP00000360372.3:n.481+47del
ENST00000464755.1:c.1244+47del	ENSP00000483243.1:n.1244+47del
ENST00000480405.2:c.*39del	ENSP00000483847.1:n.*39del
NM_000769.2:c.481+47del	NP_000760.1:n.481+47del
NM_000769.4:c.481+47del MANE Select	NP_000760.1:n.481+47del