Canonical Allele Identifier: CA2762537023
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008544G>C , CM000666.2:g.88008544G>C GRCh38
NC_000004.11:g.88929696G>C , CM000666.1:g.88929696G>C GRCh37
NC_000004.10:g.89148720G>C NCBI36
NG_008604.1:g.5877G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+216G>C MANE Select ENSP00000237596.2:n.595+216G>C
ENST00000237596.6:c.595+216G>C ENSP00000237596.2:n.595+216G>C
ENST00000506727.1:n.97+216G>C
NM_000297.3:c.595+216G>C NP_000288.1:n.595+216G>C
XM_011532028.1:c.595+216G>C XP_011530330.1:n.595+216G>C
XR_244632.2:n.690+216G>C
NR_156488.1:n.682+216G>C
XM_011532028.2:c.595+216G>C XP_011530330.1:n.595+216G>C
NM_000297.4:c.595+216G>C MANE Select NP_000288.1:n.595+216G>C
NR_156488.2:n.694+216G>C