Canonical Allele Identifier: CA2671365059
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007674del , CM000666.2:g.88007674del GRCh38
NC_000004.11:g.88928826del , CM000666.1:g.88928826del GRCh37
NC_000004.10:g.89147850del NCBI36
NG_008604.1:g.5007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-60del MANE Select ENSP00000237596.2:n.-60del
ENST00000237596.6:c.-60del ENSP00000237596.2:n.-60del
NM_000297.3:c.-60del NP_000288.1:n.-60del
XM_011532028.1:c.-60del XP_011530330.1:n.-60del
XR_244632.2:n.36del
NR_156488.1:n.28del
XM_011532028.2:c.-60del XP_011530330.1:n.-60del
NM_000297.4:c.-60del MANE Select NP_000288.1:n.-60del
NR_156488.2:n.40del