Canonical Allele Identifier: CA357615419
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88043249G>A , CM000666.2:g.88043249G>A GRCh38
NC_000004.11:g.88964401G>A , CM000666.1:g.88964401G>A GRCh37
NC_000004.10:g.89183425G>A NCBI36
NG_008604.1:g.40582G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1111G>A MANE Select ENSP00000237596.2:p.Glu371Lys
ENST00000237596.6:c.1111G>A ENSP00000237596.2:p.Glu371Lys
ENST00000506367.1:n.558G>A
NM_000297.3:c.1111G>A NP_000288.1:p.Glu371Lys
XM_011532028.1:c.1095-3393G>A XP_011530330.1:n.1095-3393G>A
XM_011532029.1:c.391G>A XP_011530331.1:p.Glu131Lys
XM_011532030.1:c.271G>A XP_011530332.1:p.Glu91Lys
XR_244632.2:n.1206G>A
NR_156488.1:n.1198G>A
XM_011532028.2:c.1095-3393G>A XP_011530330.1:n.1095-3393G>A
XM_011532030.2:c.271G>A XP_011530332.1:p.Glu91Lys
NM_000297.4:c.1111G>A MANE Select NP_000288.1:p.Glu371Lys
NR_156488.2:n.1210G>A