Canonical Allele Identifier: CA2695203465
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007942del , CM000666.2:g.88007942del GRCh38
NC_000004.11:g.88929094del , CM000666.1:g.88929094del GRCh37
NC_000004.10:g.89148118del NCBI36
NG_008604.1:g.5275del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.209del MANE Select ENSP00000237596.2:p.Gly70GlufsTer?
ENST00000237596.6:c.209del ENSP00000237596.2:p.Gly70GlufsTer?
NM_000297.3:c.209del NP_000288.1:p.Gly70GlufsTer?
XM_011532028.1:c.209del XP_011530330.1:p.Gly70GlufsTer?
XR_244632.2:n.304del
NR_156488.1:n.296del
XM_011532028.2:c.209del XP_011530330.1:p.Gly70GlufsTer?
NM_000297.4:c.209del MANE Select NP_000288.1:p.Gly70GlufsTer?
NR_156488.2:n.308del