Canonical Allele Identifier: CA1474592323
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88074822C= , CM000666.2:g.88074822C= GRCh38
NC_000004.11:g.88995974C= , CM000666.1:g.88995974C= GRCh37
NC_000004.10:g.89214998C= NCBI36
NG_008604.1:g.72155C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.2533C= MANE Select ENSP00000237596.2:p.Arg845=
ENST00000237596.6:c.2533C= ENSP00000237596.2:p.Arg845=
ENST00000502363.1:c.787C= ENSP00000425289.1:p.Arg263=
ENST00000508588.5:c.787C= ENSP00000427131.1:p.Arg263=
ENST00000511337.5:n.785C=
ENST00000512858.1:n.1011C=
NM_000297.3:c.2533C= NP_000288.1:p.Arg845=
XM_011532028.1:c.2308C= XP_011530330.1:p.Arg770=
XM_011532029.1:c.1813C= XP_011530331.1:p.Arg605=
XM_011532030.1:c.1693C= XP_011530332.1:p.Arg565=
NR_156488.1:n.2499C=
XM_011532028.2:c.2308C= XP_011530330.1:p.Arg770=
XM_011532030.2:c.1693C= XP_011530332.1:p.Arg565=
NM_000297.4:c.2533C= MANE Select NP_000288.1:p.Arg845=
NR_156488.2:n.2511C=