Canonical Allele Identifier: CA2671365269
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008378_88008387dup , CM000666.2:g.88008378_88008387dup GRCh38
NC_000004.11:g.88929530_88929539dup , CM000666.1:g.88929530_88929539dup GRCh37
NC_000004.10:g.89148554_89148563dup NCBI36
NG_008604.1:g.5711_5720dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+50_595+59dup MANE Select ENSP00000237596.2:n.595+50_595+59dup
ENST00000237596.6:c.595+50_595+59dup ENSP00000237596.2:n.595+50_595+59dup
ENST00000506727.1:n.97+50_97+59dup
NM_000297.3:c.595+50_595+59dup NP_000288.1:n.595+50_595+59dup
XM_011532028.1:c.595+50_595+59dup XP_011530330.1:n.595+50_595+59dup
XR_244632.2:n.690+50_690+59dup
NR_156488.1:n.682+50_682+59dup
XM_011532028.2:c.595+50_595+59dup XP_011530330.1:n.595+50_595+59dup
NM_000297.4:c.595+50_595+59dup MANE Select NP_000288.1:n.595+50_595+59dup
NR_156488.2:n.694+50_694+59dup