Canonical Allele Identifier: CA1474562479
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008367A= , CM000666.2:g.88008367A= GRCh38
NC_000004.11:g.88929519A= , CM000666.1:g.88929519A= GRCh37
NC_000004.10:g.89148543A= NCBI36
NG_008604.1:g.5700A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+39A= MANE Select ENSP00000237596.2:n.595+39A=
ENST00000237596.6:c.595+39A= ENSP00000237596.2:n.595+39A=
ENST00000506727.1:n.97+39A=
NM_000297.3:c.595+39A= NP_000288.1:n.595+39A=
XM_011532028.1:c.595+39A= XP_011530330.1:n.595+39A=
XR_244632.2:n.690+39A=
NR_156488.1:n.682+39A=
XM_011532028.2:c.595+39A= XP_011530330.1:n.595+39A=
NM_000297.4:c.595+39A= MANE Select NP_000288.1:n.595+39A=
NR_156488.2:n.694+39A=