Canonical Allele Identifier: CA2519036634
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008388_88008389insA , CM000666.2:g.88008388_88008389insA GRCh38
NC_000004.11:g.88929540_88929541insA , CM000666.1:g.88929540_88929541insA GRCh37
NC_000004.10:g.89148564_89148565insA NCBI36
NG_008604.1:g.5721_5722insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+60_595+61insA MANE Select ENSP00000237596.2:n.595+60_595+61insA
ENST00000237596.6:c.595+60_595+61insA ENSP00000237596.2:n.595+60_595+61insA
ENST00000506727.1:n.97+60_97+61insA
NM_000297.3:c.595+60_595+61insA NP_000288.1:n.595+60_595+61insA
XM_011532028.1:c.595+60_595+61insA XP_011530330.1:n.595+60_595+61insA
XR_244632.2:n.690+60_690+61insA
NR_156488.1:n.682+60_682+61insA
XM_011532028.2:c.595+60_595+61insA XP_011530330.1:n.595+60_595+61insA
NM_000297.4:c.595+60_595+61insA MANE Select NP_000288.1:n.595+60_595+61insA
NR_156488.2:n.694+60_694+61insA