Canonical Allele Identifier: CA1474562579
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008536_88008537delinsAT , CM000666.2:g.88008536_88008537delinsAT GRCh38
NC_000004.11:g.88929688_88929689delinsAT , CM000666.1:g.88929688_88929689delinsAT GRCh37
NC_000004.10:g.89148712_89148713delinsAT NCBI36
NG_008604.1:g.5869_5870delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+208_595+209delinsAT MANE Select ENSP00000237596.2:n.595+208_595+209delinsAT
ENST00000237596.6:c.595+208_595+209delinsAT ENSP00000237596.2:n.595+208_595+209delinsAT
ENST00000506727.1:n.97+208_97+209delinsAT
NM_000297.3:c.595+208_595+209delinsAT NP_000288.1:n.595+208_595+209delinsAT
XM_011532028.1:c.595+208_595+209delinsAT XP_011530330.1:n.595+208_595+209delinsAT
XR_244632.2:n.690+208_690+209delinsAT
NR_156488.1:n.682+208_682+209delinsAT
XM_011532028.2:c.595+208_595+209delinsAT XP_011530330.1:n.595+208_595+209delinsAT
NM_000297.4:c.595+208_595+209delinsAT MANE Select NP_000288.1:n.595+208_595+209delinsAT
NR_156488.2:n.694+208_694+209delinsAT