Canonical Allele Identifier: CA2216725879

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753471_30753472delinsAG , CM000678.2:g.30753471_30753472delinsAG	GRCh38
NC_000016.9:g.30764792_30764793delinsAG , CM000678.1:g.30764792_30764793delinsAG	GRCh37
NC_000016.8:g.30672293_30672294delinsAG	NCBI36
NG_016616.1:g.10173_10174delinsAG
NG_016616.2:g.10173_10174delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.470_471delinsAG MANE Select	ENSP00000455607.1:p.Glu157=
ENST00000328273.11:c.470_471delinsAG	ENSP00000329968.7:p.Glu157=
ENST00000424889.7:c.470_471delinsAG	ENSP00000388571.3:p.Glu157=
ENST00000561712.1:c.144_145delinsAG
ENST00000563588.5:c.470_471delinsAG	ENSP00000455607.1:p.Glu157=
ENST00000563607.1:c.*142_*143delinsAG	ENSP00000454641.1:n.*142_*143delinsAG
ENST00000563913.5:n.803_804delinsAG
ENST00000564838.5:n.844_845delinsAG
ENST00000565897.5:c.470_471delinsAG	ENSP00000457359.1:p.Glu157=
ENST00000565924.5:c.470_471delinsAG	ENSP00000455091.1:p.Glu157=
ENST00000569684.1:n.882_883delinsAG
NM_000294.2:c.470_471delinsAG	NP_000285.1:p.Glu157=
NM_001172432.1:c.470_471delinsAG	NP_001165903.1:p.Glu157=
NM_000294.3:c.470_471delinsAG MANE Select	NP_000285.1:p.Glu157=
NM_001172432.2:c.470_471delinsAG	NP_001165903.1:p.Glu157=