Canonical Allele Identifier: CA2806482178
Gene: PHKG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30753655_30753656insCACCCAAACACACCCAACAC , CM000678.2:g.30753655_30753656insCACCCAAACACACCCAACAC GRCh38
NC_000016.9:g.30764976_30764977insCACCCAAACACACCCAACAC , CM000678.1:g.30764976_30764977insCACCCAAACACACCCAACAC GRCh37
NC_000016.8:g.30672477_30672478insCACCCAAACACACCCAACAC NCBI36
NG_016616.1:g.10357_10358insCACCCAAACACACCCAACAC
NG_016616.2:g.10357_10358insCACCCAAACACACCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000563588.6:c.556+98_556+99insCACCCAAACACACCCAACAC MANE Select ENSP00000455607.1:n.556+98_556+99insCACCCAAACACACCCAACAC
ENST00000328273.11:c.556+98_556+99insCACCCAAACACACCCAACAC ENSP00000329968.7:n.556+98_556+99insCACCCAAACACACCCAACAC
ENST00000424889.7:c.556+98_556+99insCACCCAAACACACCCAACAC ENSP00000388571.3:n.556+98_556+99insCACCCAAACACACCCAACAC
ENST00000561712.1:c.230+98_230+99insCACCCAAACACACCCAACAC
ENST00000563588.5:c.556+98_556+99insCACCCAAACACACCCAACAC ENSP00000455607.1:n.556+98_556+99insCACCCAAACACACCCAACAC
ENST00000563913.5:n.889+98_889+99insCACCCAAACACACCCAACAC
ENST00000564838.5:n.930+98_930+99insCACCCAAACACACCCAACAC
ENST00000565897.5:c.556+98_556+99insCACCCAAACACACCCAACAC ENSP00000457359.1:n.556+98_556+99insCACCCAAACACACCCAACAC
ENST00000565924.5:c.556+98_556+99insCACCCAAACACACCCAACAC ENSP00000455091.1:n.556+98_556+99insCACCCAAACACACCCAACAC
ENST00000569684.1:n.968+98_968+99insCACCCAAACACACCCAACAC
NM_000294.2:c.556+98_556+99insCACCCAAACACACCCAACAC NP_000285.1:n.556+98_556+99insCACCCAAACACACCCAACAC
NM_001172432.1:c.556+98_556+99insCACCCAAACACACCCAACAC NP_001165903.1:n.556+98_556+99insCACCCAAACACACCCAACAC
NM_000294.3:c.556+98_556+99insCACCCAAACACACCCAACAC MANE Select NP_000285.1:n.556+98_556+99insCACCCAAACACACCCAACAC
NM_001172432.2:c.556+98_556+99insCACCCAAACACACCCAACAC NP_001165903.1:n.556+98_556+99insCACCCAAACACACCCAACAC