Canonical Allele Identifier: CA1474562431
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008293T= , CM000666.2:g.88008293T= GRCh38
NC_000004.11:g.88929445T= , CM000666.1:g.88929445T= GRCh37
NC_000004.10:g.89148469T= NCBI36
NG_008604.1:g.5626T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.560T= MANE Select ENSP00000237596.2:p.Val187=
ENST00000237596.6:c.560T= ENSP00000237596.2:p.Val187=
ENST00000506727.1:n.62T=
NM_000297.3:c.560T= NP_000288.1:p.Val187=
XM_011532028.1:c.560T= XP_011530330.1:p.Val187=
XR_244632.2:n.655T=
NR_156488.1:n.647T=
XM_011532028.2:c.560T= XP_011530330.1:p.Val187=
NM_000297.4:c.560T= MANE Select NP_000288.1:p.Val187=
NR_156488.2:n.659T=