Canonical Allele Identifier: CA2762537800
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038233_88038234insTTTTTT , CM000666.2:g.88038233_88038234insTTTTTT GRCh38
NC_000004.11:g.88959385_88959386insTTTTTT , CM000666.1:g.88959385_88959386insTTTTTT GRCh37
NC_000004.10:g.89178409_89178410insTTTTTT NCBI36
NG_008604.1:g.35566_35567insTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.844-18_844-17insTTTTTT MANE Select ENSP00000237596.2:n.844-18_844-17insTTTTTT
ENST00000237596.6:c.844-18_844-17insTTTTTT ENSP00000237596.2:n.844-18_844-17insTTTTTT
ENST00000506367.1:n.291-18_291-17insTTTTTT
ENST00000506727.1:n.430-18_430-17insTTTTTT
NM_000297.3:c.844-18_844-17insTTTTTT NP_000288.1:n.844-18_844-17insTTTTTT
XM_011532028.1:c.844-18_844-17insTTTTTT XP_011530330.1:n.844-18_844-17insTTTTTT
XM_011532029.1:c.124-18_124-17insTTTTTT XP_011530331.1:n.124-18_124-17insTTTTTT
XM_011532030.1:c.4-18_4-17insTTTTTT XP_011530332.1:n.4-18_4-17insTTTTTT
XR_244632.2:n.939-18_939-17insTTTTTT
NR_156488.1:n.931-18_931-17insTTTTTT
XM_011532028.2:c.844-18_844-17insTTTTTT XP_011530330.1:n.844-18_844-17insTTTTTT
XM_011532030.2:c.4-18_4-17insTTTTTT XP_011530332.1:n.4-18_4-17insTTTTTT
NM_000297.4:c.844-18_844-17insTTTTTT MANE Select NP_000288.1:n.844-18_844-17insTTTTTT
NR_156488.2:n.943-18_943-17insTTTTTT