Canonical Allele Identifier: CA1474575890
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038502G= , CM000666.2:g.88038502G= GRCh38
NC_000004.11:g.88959654G= , CM000666.1:g.88959654G= GRCh37
NC_000004.10:g.89178678G= NCBI36
NG_008604.1:g.35835G=

Transcript Alleles

HGVS Amino-acid Change
NM_000297.4:c.1094+1G= MANE Select NP_000288.1:n.1094+1G=
ENST00000237596.7:c.1094+1G= MANE Select ENSP00000237596.2:n.1094+1G=
NM_000297.3:c.1094+1G= NP_000288.1:n.1094+1G=
NR_156488.1:n.1181+1G=
NR_156488.2:n.1193+1G=
ENST00000237596.6:c.1094+1G= ENSP00000237596.2:n.1094+1G=
ENST00000506367.1:n.541+1G=
XM_011532028.1:c.1094+1G= XP_011530330.1:n.1094+1G=
XM_011532028.2:c.1094+1G= XP_011530330.1:n.1094+1G=
XM_011532029.1:c.374+1G= XP_011530331.1:n.374+1G=
XM_011532030.1:c.254+1G= XP_011530332.1:n.254+1G=
XM_011532030.2:c.254+1G= XP_011530332.1:n.254+1G=
XR_244632.2:n.1189+1G=