Canonical Allele Identifier: CA440269264
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88036353G>A , CM000666.2:g.88036353G>A GRCh38
NC_000004.11:g.88957505G>A , CM000666.1:g.88957505G>A GRCh37
NC_000004.10:g.89176529G>A NCBI36
NG_008604.1:g.33686G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.843G>A MANE Select ENSP00000237596.2:p.Lys281=
ENST00000237596.6:c.843G>A ENSP00000237596.2:p.Lys281=
ENST00000506367.1:n.290G>A
ENST00000506727.1:n.429G>A
NM_000297.3:c.843G>A NP_000288.1:p.Lys281=
XM_011532028.1:c.843G>A XP_011530330.1:p.Lys281=
XM_011532029.1:c.123G>A XP_011530331.1:p.Lys41=
XR_244632.2:n.938G>A
NR_156488.1:n.930G>A
XM_011532028.2:c.843G>A XP_011530330.1:p.Lys281=
XM_011532030.2:c.-125G>A XP_011530332.1:n.-125G>A
NM_000297.4:c.843G>A MANE Select NP_000288.1:p.Lys281=
NR_156488.2:n.942G>A