Canonical Allele Identifier: CA2671365069
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007684_88007707del , CM000666.2:g.88007684_88007707del GRCh38
NC_000004.11:g.88928836_88928859del , CM000666.1:g.88928836_88928859del GRCh37
NC_000004.10:g.89147860_89147883del NCBI36
NG_008604.1:g.5017_5040del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-50_-27del MANE Select ENSP00000237596.2:n.-50_-27del
ENST00000237596.6:c.-50_-27del ENSP00000237596.2:n.-50_-27del
NM_000297.3:c.-50_-27del NP_000288.1:n.-50_-27del
XM_011532028.1:c.-50_-27del XP_011530330.1:n.-50_-27del
XR_244632.2:n.46_69del
NR_156488.1:n.38_61del
XM_011532028.2:c.-50_-27del XP_011530330.1:n.-50_-27del
NM_000297.4:c.-50_-27del MANE Select NP_000288.1:n.-50_-27del
NR_156488.2:n.50_73del