Canonical Allele Identifier: CA2632764481

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751192_30751206del , CM000678.2:g.30751192_30751206del	GRCh38
NC_000016.9:g.30762513_30762527del , CM000678.1:g.30762513_30762527del	GRCh37
NC_000016.8:g.30670014_30670028del	NCBI36
NG_016616.1:g.7894_7908del
NG_016616.2:g.7894_7908del

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.182_196del MANE Select	NP_000285.1:p.Arg61_Glu65del
ENST00000563588.6:c.182_196del MANE Select	ENSP00000455607.1:p.Arg61_Glu65del
NM_000294.2:c.182_196del	NP_000285.1:p.Arg61_Glu65del
NM_001172432.1:c.182_196del	NP_001165903.1:p.Arg61_Glu65del
NM_001172432.2:c.182_196del	NP_001165903.1:p.Arg61_Glu65del
ENST00000328273.11:c.182_196del	ENSP00000329968.7:p.Arg61_Glu65del
ENST00000424889.7:c.182_196del	ENSP00000388571.3:p.Arg61_Glu65del
ENST00000563588.5:c.182_196del	ENSP00000455607.1:p.Arg61_Glu65del
ENST00000563607.1:c.182_196del	ENSP00000454641.1:p.Arg61_Glu65del
ENST00000563913.5:n.248_262del
ENST00000564838.5:n.289_303del
ENST00000565897.5:c.182_196del	ENSP00000457359.1:p.Arg61_Glu65del
ENST00000565924.5:c.182_196del	ENSP00000455091.1:p.Arg61_Glu65del
ENST00000569762.1:n.159_173del