Canonical Allele Identifier: CA2671365179
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007797_88007798insT , CM000666.2:g.88007797_88007798insT GRCh38
NC_000004.11:g.88928949_88928950insT , CM000666.1:g.88928949_88928950insT GRCh37
NC_000004.10:g.89147973_89147974insT NCBI36
NG_008604.1:g.5130_5131insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.64_65insT MANE Select ENSP00000237596.2:p.Arg22LeufsTer?
ENST00000237596.6:c.64_65insT ENSP00000237596.2:p.Arg22LeufsTer?
NM_000297.3:c.64_65insT NP_000288.1:p.Arg22LeufsTer?
XM_011532028.1:c.64_65insT XP_011530330.1:p.Arg22LeufsTer?
XR_244632.2:n.159_160insT
NR_156488.1:n.151_152insT
XM_011532028.2:c.64_65insT XP_011530330.1:p.Arg22LeufsTer?
NM_000297.4:c.64_65insT MANE Select NP_000288.1:p.Arg22LeufsTer?
NR_156488.2:n.163_164insT