Canonical Allele Identifier: CA2671365178
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007791del , CM000666.2:g.88007791del GRCh38
NC_000004.11:g.88928943del , CM000666.1:g.88928943del GRCh37
NC_000004.10:g.89147967del NCBI36
NG_008604.1:g.5124del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.58del MANE Select ENSP00000237596.2:p.Ala20ArgfsTer10
ENST00000237596.6:c.58del ENSP00000237596.2:p.Ala20ArgfsTer10
NM_000297.3:c.58del NP_000288.1:p.Ala20ArgfsTer10
XM_011532028.1:c.58del XP_011530330.1:p.Ala20ArgfsTer10
XR_244632.2:n.153del
NR_156488.1:n.145del
XM_011532028.2:c.58del XP_011530330.1:p.Ala20ArgfsTer10
NM_000297.4:c.58del MANE Select NP_000288.1:p.Ala20ArgfsTer10
NR_156488.2:n.157del