Canonical Allele Identifier: CA1474562317
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008076G= , CM000666.2:g.88008076G= GRCh38
NC_000004.11:g.88929228G= , CM000666.1:g.88929228G= GRCh37
NC_000004.10:g.89148252G= NCBI36
NG_008604.1:g.5409G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.343G= MANE Select ENSP00000237596.2:p.Asp115=
ENST00000237596.6:c.343G= ENSP00000237596.2:p.Asp115=
NM_000297.3:c.343G= NP_000288.1:p.Asp115=
XM_011532028.1:c.343G= XP_011530330.1:p.Asp115=
XR_244632.2:n.438G=
NR_156488.1:n.430G=
XM_011532028.2:c.343G= XP_011530330.1:p.Asp115=
NM_000297.4:c.343G= MANE Select NP_000288.1:p.Asp115=
NR_156488.2:n.442G=