Canonical Allele Identifier: CA2695203543
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038380dup , CM000666.2:g.88038380dup GRCh38
NC_000004.11:g.88959532dup , CM000666.1:g.88959532dup GRCh37
NC_000004.10:g.89178556dup NCBI36
NG_008604.1:g.35713dup

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.973dup MANE Select ENSP00000237596.2:p.Arg325ProfsTer16
ENST00000237596.6:c.973dup ENSP00000237596.2:p.Arg325ProfsTer16
ENST00000506367.1:n.420dup
NM_000297.3:c.973dup NP_000288.1:p.Arg325ProfsTer16
XM_011532028.1:c.973dup XP_011530330.1:p.Arg325ProfsTer16
XM_011532029.1:c.253dup XP_011530331.1:p.Arg85ProfsTer16
XM_011532030.1:c.133dup XP_011530332.1:p.Arg45ProfsTer16
XR_244632.2:n.1068dup
NR_156488.1:n.1060dup
XM_011532028.2:c.973dup XP_011530330.1:p.Arg325ProfsTer16
XM_011532030.2:c.133dup XP_011530332.1:p.Arg45ProfsTer16
NM_000297.4:c.973dup MANE Select NP_000288.1:p.Arg325ProfsTer16
NR_156488.2:n.1072dup