Canonical Allele Identifier: CA1474562458
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008331_88008333delinsAAG , CM000666.2:g.88008331_88008333delinsAAG GRCh38
NC_000004.11:g.88929483_88929485delinsAAG , CM000666.1:g.88929483_88929485delinsAAG GRCh37
NC_000004.10:g.89148507_89148509delinsAAG NCBI36
NG_008604.1:g.5664_5666delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+3_595+5delinsAAG MANE Select ENSP00000237596.2:n.595+3_595+5delinsAAG
ENST00000237596.6:c.595+3_595+5delinsAAG ENSP00000237596.2:n.595+3_595+5delinsAAG
ENST00000506727.1:n.97+3_97+5delinsAAG
NM_000297.3:c.595+3_595+5delinsAAG NP_000288.1:n.595+3_595+5delinsAAG
XM_011532028.1:c.595+3_595+5delinsAAG XP_011530330.1:n.595+3_595+5delinsAAG
XR_244632.2:n.690+3_690+5delinsAAG
NR_156488.1:n.682+3_682+5delinsAAG
XM_011532028.2:c.595+3_595+5delinsAAG XP_011530330.1:n.595+3_595+5delinsAAG
NM_000297.4:c.595+3_595+5delinsAAG MANE Select NP_000288.1:n.595+3_595+5delinsAAG
NR_156488.2:n.694+3_694+5delinsAAG