Canonical Allele Identifier: CA357632876
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038391T>A , CM000666.2:g.88038391T>A GRCh38
NC_000004.11:g.88959543T>A , CM000666.1:g.88959543T>A GRCh37
NC_000004.10:g.89178567T>A NCBI36
NG_008604.1:g.35724T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.984T>A MANE Select ENSP00000237596.2:p.Asn328Lys
ENST00000237596.6:c.984T>A ENSP00000237596.2:p.Asn328Lys
ENST00000506367.1:n.431T>A
NM_000297.3:c.984T>A NP_000288.1:p.Asn328Lys
XM_011532028.1:c.984T>A XP_011530330.1:p.Asn328Lys
XM_011532029.1:c.264T>A XP_011530331.1:p.Asn88Lys
XM_011532030.1:c.144T>A XP_011530332.1:p.Asn48Lys
XR_244632.2:n.1079T>A
NR_156488.1:n.1071T>A
XM_011532028.2:c.984T>A XP_011530330.1:p.Asn328Lys
XM_011532030.2:c.144T>A XP_011530332.1:p.Asn48Lys
NM_000297.4:c.984T>A MANE Select NP_000288.1:p.Asn328Lys
NR_156488.2:n.1083T>A