Canonical Allele Identifier: CA2762537801
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038246T>G , CM000666.2:g.88038246T>G GRCh38
NC_000004.11:g.88959398T>G , CM000666.1:g.88959398T>G GRCh37
NC_000004.10:g.89178422T>G NCBI36
NG_008604.1:g.35579T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.844-5T>G MANE Select ENSP00000237596.2:n.844-5T>G
ENST00000237596.6:c.844-5T>G ENSP00000237596.2:n.844-5T>G
ENST00000506367.1:n.291-5T>G
ENST00000506727.1:n.430-5T>G
NM_000297.3:c.844-5T>G NP_000288.1:n.844-5T>G
XM_011532028.1:c.844-5T>G XP_011530330.1:n.844-5T>G
XM_011532029.1:c.124-5T>G XP_011530331.1:n.124-5T>G
XM_011532030.1:c.4-5T>G XP_011530332.1:n.4-5T>G
XR_244632.2:n.939-5T>G
NR_156488.1:n.931-5T>G
XM_011532028.2:c.844-5T>G XP_011530330.1:n.844-5T>G
XM_011532030.2:c.4-5T>G XP_011530332.1:n.4-5T>G
NM_000297.4:c.844-5T>G MANE Select NP_000288.1:n.844-5T>G
NR_156488.2:n.943-5T>G