Canonical Allele Identifier: CA2671365394
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008460_88008461insGAA , CM000666.2:g.88008460_88008461insGAA GRCh38
NC_000004.11:g.88929612_88929613insGAA , CM000666.1:g.88929612_88929613insGAA GRCh37
NC_000004.10:g.89148636_89148637insGAA NCBI36
NG_008604.1:g.5793_5794insGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+132_595+133insGAA MANE Select ENSP00000237596.2:n.595+132_595+133insGAA
ENST00000237596.6:c.595+132_595+133insGAA ENSP00000237596.2:n.595+132_595+133insGAA
ENST00000506727.1:n.97+132_97+133insGAA
NM_000297.3:c.595+132_595+133insGAA NP_000288.1:n.595+132_595+133insGAA
XM_011532028.1:c.595+132_595+133insGAA XP_011530330.1:n.595+132_595+133insGAA
XR_244632.2:n.690+132_690+133insGAA
NR_156488.1:n.682+132_682+133insGAA
XM_011532028.2:c.595+132_595+133insGAA XP_011530330.1:n.595+132_595+133insGAA
NM_000297.4:c.595+132_595+133insGAA MANE Select NP_000288.1:n.595+132_595+133insGAA
NR_156488.2:n.694+132_694+133insGAA