Canonical Allele Identifier: CA1474562357
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008146G= , CM000666.2:g.88008146G= GRCh38
NC_000004.11:g.88929298G= , CM000666.1:g.88929298G= GRCh37
NC_000004.10:g.89148322G= NCBI36
NG_008604.1:g.5479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.413G= MANE Select ENSP00000237596.2:p.Ser138=
ENST00000237596.6:c.413G= ENSP00000237596.2:p.Ser138=
NM_000297.3:c.413G= NP_000288.1:p.Ser138=
XM_011532028.1:c.413G= XP_011530330.1:p.Ser138=
XR_244632.2:n.508G=
NR_156488.1:n.500G=
XM_011532028.2:c.413G= XP_011530330.1:p.Ser138=
NM_000297.4:c.413G= MANE Select NP_000288.1:p.Ser138=
NR_156488.2:n.512G=