Canonical Allele Identifier: CA2671365092
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007695_88007696del , CM000666.2:g.88007695_88007696del GRCh38
NC_000004.11:g.88928847_88928848del , CM000666.1:g.88928847_88928848del GRCh37
NC_000004.10:g.89147871_89147872del NCBI36
NG_008604.1:g.5028_5029del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-39_-38del MANE Select ENSP00000237596.2:n.-39_-38del
ENST00000237596.6:c.-39_-38del ENSP00000237596.2:n.-39_-38del
NM_000297.3:c.-39_-38del NP_000288.1:n.-39_-38del
XM_011532028.1:c.-39_-38del XP_011530330.1:n.-39_-38del
XR_244632.2:n.57_58del
NR_156488.1:n.49_50del
XM_011532028.2:c.-39_-38del XP_011530330.1:n.-39_-38del
NM_000297.4:c.-39_-38del MANE Select NP_000288.1:n.-39_-38del
NR_156488.2:n.61_62del