Canonical Allele Identifier: CA357626965
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008249-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008249C>A , CM000666.2:g.88008249C>A GRCh38
NC_000004.11:g.88929401C>A , CM000666.1:g.88929401C>A GRCh37
NC_000004.10:g.89148425C>A NCBI36
NG_008604.1:g.5582C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.516C>A MANE Select ENSP00000237596.2:p.Asp172Glu
ENST00000237596.6:c.516C>A ENSP00000237596.2:p.Asp172Glu
ENST00000506727.1:n.18C>A
NM_000297.3:c.516C>A NP_000288.1:p.Asp172Glu
XM_011532028.1:c.516C>A XP_011530330.1:p.Asp172Glu
XR_244632.2:n.611C>A
NR_156488.1:n.603C>A
XM_011532028.2:c.516C>A XP_011530330.1:p.Asp172Glu
NM_000297.4:c.516C>A MANE Select NP_000288.1:p.Asp172Glu
NR_156488.2:n.615C>A