Canonical Allele Identifier: CA357633280
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038491A>G , CM000666.2:g.88038491A>G GRCh38
NC_000004.11:g.88959643A>G , CM000666.1:g.88959643A>G GRCh37
NC_000004.10:g.89178667A>G NCBI36
NG_008604.1:g.35824A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1084A>G MANE Select ENSP00000237596.2:p.Asn362Asp
ENST00000237596.6:c.1084A>G ENSP00000237596.2:p.Asn362Asp
ENST00000506367.1:n.531A>G
NM_000297.3:c.1084A>G NP_000288.1:p.Asn362Asp
XM_011532028.1:c.1084A>G XP_011530330.1:p.Asn362Asp
XM_011532029.1:c.364A>G XP_011530331.1:p.Asn122Asp
XM_011532030.1:c.244A>G XP_011530332.1:p.Asn82Asp
XR_244632.2:n.1179A>G
NR_156488.1:n.1171A>G
XM_011532028.2:c.1084A>G XP_011530330.1:p.Asn362Asp
XM_011532030.2:c.244A>G XP_011530332.1:p.Asn82Asp
NM_000297.4:c.1084A>G MANE Select NP_000288.1:p.Asn362Asp
NR_156488.2:n.1183A>G