Canonical Allele Identifier: CA1474562055
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007672_88007675delinsCCTG , CM000666.2:g.88007672_88007675delinsCCTG GRCh38
NC_000004.11:g.88928824_88928827delinsCCTG , CM000666.1:g.88928824_88928827delinsCCTG GRCh37
NC_000004.10:g.89147848_89147851delinsCCTG NCBI36
NG_008604.1:g.5005_5008delinsCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-62_-59delinsCCTG MANE Select ENSP00000237596.2:n.-62_-59delinsCCTG
ENST00000237596.6:c.-62_-59delinsCCTG ENSP00000237596.2:n.-62_-59delinsCCTG
NM_000297.3:c.-62_-59delinsCCTG NP_000288.1:n.-62_-59delinsCCTG
XM_011532028.1:c.-62_-59delinsCCTG XP_011530330.1:n.-62_-59delinsCCTG
XR_244632.2:n.34_37delinsCCTG
NR_156488.1:n.26_29delinsCCTG
XM_011532028.2:c.-62_-59delinsCCTG XP_011530330.1:n.-62_-59delinsCCTG
NM_000297.4:c.-62_-59delinsCCTG MANE Select NP_000288.1:n.-62_-59delinsCCTG
NR_156488.2:n.38_41delinsCCTG