Canonical Allele Identifier: CA2671365029
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007660del , CM000666.2:g.88007660del GRCh38
NC_000004.11:g.88928812del , CM000666.1:g.88928812del GRCh37
NC_000004.10:g.89147836del NCBI36
NG_008604.1:g.4993del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-74del MANE Select ENSP00000237596.2:n.-74del
NM_000297.3:c.-74del NP_000288.1:n.-74del
XM_011532028.1:c.-74del XP_011530330.1:n.-74del
XR_244632.2:n.22del
NR_156488.1:n.14del
XM_011532028.2:c.-74del XP_011530330.1:n.-74del
NM_000297.4:c.-74del MANE Select NP_000288.1:n.-74del
NR_156488.2:n.26del