Canonical Allele Identifier: CA357624900
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007774A>T , CM000666.2:g.88007774A>T GRCh38
NC_000004.11:g.88928926A>T , CM000666.1:g.88928926A>T GRCh37
NC_000004.10:g.89147950A>T NCBI36
NG_008604.1:g.5107A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.41A>T MANE Select ENSP00000237596.2:p.Asp14Val
ENST00000237596.6:c.41A>T ENSP00000237596.2:p.Asp14Val
NM_000297.3:c.41A>T NP_000288.1:p.Asp14Val
XM_011532028.1:c.41A>T XP_011530330.1:p.Asp14Val
XR_244632.2:n.136A>T
NR_156488.1:n.128A>T
XM_011532028.2:c.41A>T XP_011530330.1:p.Asp14Val
NM_000297.4:c.41A>T MANE Select NP_000288.1:p.Asp14Val
NR_156488.2:n.140A>T