Canonical Allele Identifier: CA2216719648

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751075_30751077delinsCCT , CM000678.2:g.30751075_30751077delinsCCT	GRCh38
NC_000016.9:g.30762396_30762398delinsCCT , CM000678.1:g.30762396_30762398delinsCCT	GRCh37
NC_000016.8:g.30669897_30669899delinsCCT	NCBI36
NG_016616.1:g.7777_7779delinsCCT
NG_016616.2:g.7777_7779delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.96-31_96-29delinsCCT MANE Select	NP_000285.1:n.96-31_96-29delinsCCT
ENST00000563588.6:c.96-31_96-29delinsCCT MANE Select	ENSP00000455607.1:n.96-31_96-29delinsCCT
NM_000294.2:c.96-31_96-29delinsCCT	NP_000285.1:n.96-31_96-29delinsCCT
NM_001172432.1:c.96-31_96-29delinsCCT	NP_001165903.1:n.96-31_96-29delinsCCT
NM_001172432.2:c.96-31_96-29delinsCCT	NP_001165903.1:n.96-31_96-29delinsCCT
ENST00000328273.11:c.96-31_96-29delinsCCT	ENSP00000329968.7:n.96-31_96-29delinsCCT
ENST00000424889.7:c.96-31_96-29delinsCCT	ENSP00000388571.3:n.96-31_96-29delinsCCT
ENST00000563588.5:c.96-31_96-29delinsCCT	ENSP00000455607.1:n.96-31_96-29delinsCCT
ENST00000563607.1:c.96-31_96-29delinsCCT	ENSP00000454641.1:n.96-31_96-29delinsCCT
ENST00000563913.5:n.162-31_162-29delinsCCT
ENST00000564838.5:n.203-31_203-29delinsCCT
ENST00000565897.5:c.96-31_96-29delinsCCT	ENSP00000457359.1:n.96-31_96-29delinsCCT
ENST00000565924.5:c.96-31_96-29delinsCCT	ENSP00000455091.1:n.96-31_96-29delinsCCT
ENST00000569762.1:n.73-31_73-29delinsCCT