Canonical Allele Identifier: CA2216725929

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753498A= , CM000678.2:g.30753498A=	GRCh38
NC_000016.9:g.30764819A= , CM000678.1:g.30764819A=	GRCh37
NC_000016.8:g.30672320A=	NCBI36
NG_016616.1:g.10200A=
NG_016616.2:g.10200A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.497A= MANE Select	ENSP00000455607.1:p.Gln166=
ENST00000328273.11:c.497A=	ENSP00000329968.7:p.Gln166=
ENST00000424889.7:c.497A=	ENSP00000388571.3:p.Gln166=
ENST00000561712.1:c.171A=
ENST00000563588.5:c.497A=	ENSP00000455607.1:p.Gln166=
ENST00000563607.1:c.*169A=	ENSP00000454641.1:n.*169A=
ENST00000563913.5:n.830A=
ENST00000564838.5:n.871A=
ENST00000565897.5:c.497A=	ENSP00000457359.1:p.Gln166=
ENST00000565924.5:c.497A=	ENSP00000455091.1:p.Gln166=
ENST00000569684.1:n.909A=
NM_000294.2:c.497A=	NP_000285.1:p.Gln166=
NM_001172432.1:c.497A=	NP_001165903.1:p.Gln166=
NM_000294.3:c.497A= MANE Select	NP_000285.1:p.Gln166=
NM_001172432.2:c.497A=	NP_001165903.1:p.Gln166=