Canonical Allele Identifier: CA1474562433
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008297C= , CM000666.2:g.88008297C= GRCh38
NC_000004.11:g.88929449C= , CM000666.1:g.88929449C= GRCh37
NC_000004.10:g.89148473C= NCBI36
NG_008604.1:g.5630C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.564C= MANE Select ENSP00000237596.2:p.Ala188=
ENST00000237596.6:c.564C= ENSP00000237596.2:p.Ala188=
ENST00000506727.1:n.66C=
NM_000297.3:c.564C= NP_000288.1:p.Ala188=
XM_011532028.1:c.564C= XP_011530330.1:p.Ala188=
XR_244632.2:n.659C=
NR_156488.1:n.651C=
XM_011532028.2:c.564C= XP_011530330.1:p.Ala188=
NM_000297.4:c.564C= MANE Select NP_000288.1:p.Ala188=
NR_156488.2:n.663C=