Canonical Allele Identifier: CA1474562459
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008332A= , CM000666.2:g.88008332A= GRCh38
NC_000004.11:g.88929484A= , CM000666.1:g.88929484A= GRCh37
NC_000004.10:g.89148508A= NCBI36
NG_008604.1:g.5665A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+4A= MANE Select ENSP00000237596.2:n.595+4A=
ENST00000237596.6:c.595+4A= ENSP00000237596.2:n.595+4A=
ENST00000506727.1:n.97+4A=
NM_000297.3:c.595+4A= NP_000288.1:n.595+4A=
XM_011532028.1:c.595+4A= XP_011530330.1:n.595+4A=
XR_244632.2:n.690+4A=
NR_156488.1:n.682+4A=
XM_011532028.2:c.595+4A= XP_011530330.1:n.595+4A=
NM_000297.4:c.595+4A= MANE Select NP_000288.1:n.595+4A=
NR_156488.2:n.694+4A=