Canonical Allele Identifier: CA2216725745

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753416G= , CM000678.2:g.30753416G=	GRCh38
NC_000016.9:g.30764737G= , CM000678.1:g.30764737G=	GRCh37
NC_000016.8:g.30672238G=	NCBI36
NG_016616.1:g.10118G=
NG_016616.2:g.10118G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.415G= MANE Select	ENSP00000455607.1:p.Glu139=
ENST00000328273.11:c.415G=	ENSP00000329968.7:p.Glu139=
ENST00000424889.7:c.415G=	ENSP00000388571.3:p.Glu139=
ENST00000561712.1:c.89G=
ENST00000563588.5:c.415G=	ENSP00000455607.1:p.Glu139=
ENST00000563607.1:c.*87G=	ENSP00000454641.1:n.*87G=
ENST00000563913.5:n.748G=
ENST00000564838.5:n.789G=
ENST00000565897.5:c.415G=	ENSP00000457359.1:p.Glu139=
ENST00000565924.5:c.415G=	ENSP00000455091.1:p.Glu139=
ENST00000569684.1:n.827G=
NM_000294.2:c.415G=	NP_000285.1:p.Glu139=
NM_001172432.1:c.415G=	NP_001165903.1:p.Glu139=
NM_000294.3:c.415G= MANE Select	NP_000285.1:p.Glu139=
NM_001172432.2:c.415G=	NP_001165903.1:p.Glu139=