Canonical Allele Identifier: CA8013188
Gene: PHKG2 HGNC NCBI

Linked Data

dbSNP Id: rs773199410

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30753472del , CM000678.2:g.30753472del GRCh38
NC_000016.9:g.30764793del , CM000678.1:g.30764793del GRCh37
NC_000016.8:g.30672294del NCBI36
NG_016616.1:g.10174del
NG_016616.2:g.10174del

Transcript Alleles

HGVS Amino-acid Change
ENST00000563588.6:c.471del MANE Select ENSP00000455607.1:p.Asn158IlefsTer4
ENST00000328273.11:c.471del ENSP00000329968.7:p.Asn158IlefsTer4
ENST00000424889.7:c.471del ENSP00000388571.3:p.Asn158IlefsTer4
ENST00000561712.1:c.145del
ENST00000563588.5:c.471del ENSP00000455607.1:p.Asn158IlefsTer4
ENST00000563607.1:c.*143del ENSP00000454641.1:n.*143del
ENST00000563913.5:n.804del
ENST00000564838.5:n.845del
ENST00000565897.5:c.471del ENSP00000457359.1:p.Asn158IlefsTer4
ENST00000565924.5:c.471del ENSP00000455091.1:p.Asn158IlefsTer4
ENST00000569684.1:n.883del
NM_000294.2:c.471del NP_000285.1:p.Asn158IlefsTer4
NM_001172432.1:c.471del NP_001165903.1:p.Asn158IlefsTer4
NM_000294.3:c.471del MANE Select NP_000285.1:p.Asn158IlefsTer4
NM_001172432.2:c.471del NP_001165903.1:p.Asn158IlefsTer4