Canonical Allele Identifier: CA2671365149
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007720_88007721insCCGG , CM000666.2:g.88007720_88007721insCCGG GRCh38
NC_000004.11:g.88928872_88928873insCCGG , CM000666.1:g.88928872_88928873insCCGG GRCh37
NC_000004.10:g.89147896_89147897insCCGG NCBI36
NG_008604.1:g.5053_5054insCCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-14_-13insCCGG MANE Select ENSP00000237596.2:n.-14_-13insCCGG
ENST00000237596.6:c.-14_-13insCCGG ENSP00000237596.2:n.-14_-13insCCGG
NM_000297.3:c.-14_-13insCCGG NP_000288.1:n.-14_-13insCCGG
XM_011532028.1:c.-14_-13insCCGG XP_011530330.1:n.-14_-13insCCGG
XR_244632.2:n.82_83insCCGG
NR_156488.1:n.74_75insCCGG
XM_011532028.2:c.-14_-13insCCGG XP_011530330.1:n.-14_-13insCCGG
NM_000297.4:c.-14_-13insCCGG MANE Select NP_000288.1:n.-14_-13insCCGG
NR_156488.2:n.86_87insCCGG