Canonical Allele Identifier: CA1474562443
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008314T= , CM000666.2:g.88008314T= GRCh38
NC_000004.11:g.88929466T= , CM000666.1:g.88929466T= GRCh37
NC_000004.10:g.89148490T= NCBI36
NG_008604.1:g.5647T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.581T= MANE Select ENSP00000237596.2:p.Val194=
ENST00000237596.6:c.581T= ENSP00000237596.2:p.Val194=
ENST00000506727.1:n.83T=
NM_000297.3:c.581T= NP_000288.1:p.Val194=
XM_011532028.1:c.581T= XP_011530330.1:p.Val194=
XR_244632.2:n.676T=
NR_156488.1:n.668T=
XM_011532028.2:c.581T= XP_011530330.1:p.Val194=
NM_000297.4:c.581T= MANE Select NP_000288.1:p.Val194=
NR_156488.2:n.680T=