Canonical Allele Identifier: CA2671365170
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007764del , CM000666.2:g.88007764del GRCh38
NC_000004.11:g.88928916del , CM000666.1:g.88928916del GRCh37
NC_000004.10:g.89147940del NCBI36
NG_008604.1:g.5097del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.31del MANE Select ENSP00000237596.2:p.Gln11SerfsTer19
ENST00000237596.6:c.31del ENSP00000237596.2:p.Gln11SerfsTer19
NM_000297.3:c.31del NP_000288.1:p.Gln11SerfsTer19
XM_011532028.1:c.31del XP_011530330.1:p.Gln11SerfsTer19
XR_244632.2:n.126del
NR_156488.1:n.118del
XM_011532028.2:c.31del XP_011530330.1:p.Gln11SerfsTer19
NM_000297.4:c.31del MANE Select NP_000288.1:p.Gln11SerfsTer19
NR_156488.2:n.130del