Canonical Allele Identifier: CA2695203480
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008204dup , CM000666.2:g.88008204dup GRCh38
NC_000004.11:g.88929356dup , CM000666.1:g.88929356dup GRCh37
NC_000004.10:g.89148380dup NCBI36
NG_008604.1:g.5537dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.471dup MANE Select ENSP00000237596.2:p.Glu158ArgfsTer?
ENST00000237596.6:c.471dup ENSP00000237596.2:p.Glu158ArgfsTer?
NM_000297.3:c.471dup NP_000288.1:p.Glu158ArgfsTer?
XM_011532028.1:c.471dup XP_011530330.1:p.Glu158ArgfsTer?
XR_244632.2:n.566dup
NR_156488.1:n.558dup
XM_011532028.2:c.471dup XP_011530330.1:p.Glu158ArgfsTer?
NM_000297.4:c.471dup MANE Select NP_000288.1:p.Glu158ArgfsTer?
NR_156488.2:n.570dup