Canonical Allele Identifier: CA1474575840
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038385C= , CM000666.2:g.88038385C= GRCh38
NC_000004.11:g.88959537C= , CM000666.1:g.88959537C= GRCh37
NC_000004.10:g.89178561C= NCBI36
NG_008604.1:g.35718C=

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.978C= MANE Select ENSP00000237596.2:p.Val326=
ENST00000237596.6:c.978C= ENSP00000237596.2:p.Val326=
ENST00000506367.1:n.425C=
NM_000297.3:c.978C= NP_000288.1:p.Val326=
XM_011532028.1:c.978C= XP_011530330.1:p.Val326=
XM_011532029.1:c.258C= XP_011530331.1:p.Val86=
XM_011532030.1:c.138C= XP_011530332.1:p.Val46=
XR_244632.2:n.1073C=
NR_156488.1:n.1065C=
XM_011532028.2:c.978C= XP_011530330.1:p.Val326=
XM_011532030.2:c.138C= XP_011530332.1:p.Val46=
NM_000297.4:c.978C= MANE Select NP_000288.1:p.Val326=
NR_156488.2:n.1077C=