Canonical Allele Identifier: CA1474562214
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007881_88007882delinsCG , CM000666.2:g.88007881_88007882delinsCG GRCh38
NC_000004.11:g.88929033_88929034delinsCG , CM000666.1:g.88929033_88929034delinsCG GRCh37
NC_000004.10:g.89148057_89148058delinsCG NCBI36
NG_008604.1:g.5214_5215delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.148_149delinsCG MANE Select ENSP00000237596.2:p.Arg50=
ENST00000237596.6:c.148_149delinsCG ENSP00000237596.2:p.Arg50=
NM_000297.3:c.148_149delinsCG NP_000288.1:p.Arg50=
XM_011532028.1:c.148_149delinsCG XP_011530330.1:p.Arg50=
XR_244632.2:n.243_244delinsCG
NR_156488.1:n.235_236delinsCG
XM_011532028.2:c.148_149delinsCG XP_011530330.1:p.Arg50=
NM_000297.4:c.148_149delinsCG MANE Select NP_000288.1:p.Arg50=
NR_156488.2:n.247_248delinsCG