Canonical Allele Identifier: CA1474579574
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88046712C= , CM000666.2:g.88046712C= GRCh38
NC_000004.11:g.88967864C= , CM000666.1:g.88967864C= GRCh37
NC_000004.10:g.89186888C= NCBI36
NG_008604.1:g.44045C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1390C= MANE Select ENSP00000237596.2:p.Arg464=
ENST00000237596.6:c.1390C= ENSP00000237596.2:p.Arg464=
ENST00000508588.5:c.-199+3255C= ENSP00000427131.1:n.-199+3255C=
NM_000297.3:c.1390C= NP_000288.1:p.Arg464=
XM_011532028.1:c.1165C= XP_011530330.1:p.Arg389=
XM_011532029.1:c.670C= XP_011530331.1:p.Arg224=
XM_011532030.1:c.550C= XP_011530332.1:p.Arg184=
XR_244632.2:n.1485C=
NR_156488.1:n.1477C=
XM_011532028.2:c.1165C= XP_011530330.1:p.Arg389=
XM_011532030.2:c.550C= XP_011530332.1:p.Arg184=
NM_000297.4:c.1390C= MANE Select NP_000288.1:p.Arg464=
NR_156488.2:n.1489C=