Canonical Allele Identifier: CA2841631957

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753290dup , CM000678.2:g.30753290dup	GRCh38
NC_000016.9:g.30764611dup , CM000678.1:g.30764611dup	GRCh37
NC_000016.8:g.30672112dup	NCBI36
NG_016616.1:g.9992dup
NG_016616.2:g.9992dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.385dup MANE Select	ENSP00000455607.1:p.Glu129GlyfsTer?
ENST00000328273.11:c.385dup	ENSP00000329968.7:p.Glu129GlyfsTer?
ENST00000424889.7:c.385dup	ENSP00000388571.3:p.Glu129GlyfsTer?
ENST00000561712.1:c.59dup
ENST00000563588.5:c.385dup	ENSP00000455607.1:p.Glu129GlyfsTer?
ENST00000563607.1:c.*57dup	ENSP00000454641.1:n.*57dup
ENST00000563913.5:n.718dup
ENST00000564838.5:n.759dup
ENST00000565897.5:c.385dup	ENSP00000457359.1:p.Glu129GlyfsTer?
ENST00000565924.5:c.385dup	ENSP00000455091.1:p.Glu129GlyfsTer?
ENST00000569684.1:n.797dup
NM_000294.2:c.385dup	NP_000285.1:p.Glu129GlyfsTer?
NM_001172432.1:c.385dup	NP_001165903.1:p.Glu129GlyfsTer?
NM_000294.3:c.385dup MANE Select	NP_000285.1:p.Glu129GlyfsTer?
NM_001172432.2:c.385dup	NP_001165903.1:p.Glu129GlyfsTer?