Canonical Allele Identifier: CA357626979
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008253-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008253C>A , CM000666.2:g.88008253C>A GRCh38
NC_000004.11:g.88929405C>A , CM000666.1:g.88929405C>A GRCh37
NC_000004.10:g.89148429C>A NCBI36
NG_008604.1:g.5586C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.520C>A MANE Select ENSP00000237596.2:p.Leu174Met
ENST00000237596.6:c.520C>A ENSP00000237596.2:p.Leu174Met
ENST00000506727.1:n.22C>A
NM_000297.3:c.520C>A NP_000288.1:p.Leu174Met
XM_011532028.1:c.520C>A XP_011530330.1:p.Leu174Met
XR_244632.2:n.615C>A
NR_156488.1:n.607C>A
XM_011532028.2:c.520C>A XP_011530330.1:p.Leu174Met
NM_000297.4:c.520C>A MANE Select NP_000288.1:p.Leu174Met
NR_156488.2:n.619C>A