Canonical Allele Identifier: CA2671365091
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007694_88007705del , CM000666.2:g.88007694_88007705del GRCh38
NC_000004.11:g.88928846_88928857del , CM000666.1:g.88928846_88928857del GRCh37
NC_000004.10:g.89147870_89147881del NCBI36
NG_008604.1:g.5027_5038del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-40_-29del MANE Select ENSP00000237596.2:n.-40_-29del
ENST00000237596.6:c.-40_-29del ENSP00000237596.2:n.-40_-29del
NM_000297.3:c.-40_-29del NP_000288.1:n.-40_-29del
XM_011532028.1:c.-40_-29del XP_011530330.1:n.-40_-29del
XR_244632.2:n.56_67del
NR_156488.1:n.48_59del
XM_011532028.2:c.-40_-29del XP_011530330.1:n.-40_-29del
NM_000297.4:c.-40_-29del MANE Select NP_000288.1:n.-40_-29del
NR_156488.2:n.60_71del