Canonical Allele Identifier: CA1474562165
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007793G= , CM000666.2:g.88007793G= GRCh38
NC_000004.11:g.88928945G= , CM000666.1:g.88928945G= GRCh37
NC_000004.10:g.89147969G= NCBI36
NG_008604.1:g.5126G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.60G= MANE Select ENSP00000237596.2:p.Ala20=
ENST00000237596.6:c.60G= ENSP00000237596.2:p.Ala20=
NM_000297.3:c.60G= NP_000288.1:p.Ala20=
XM_011532028.1:c.60G= XP_011530330.1:p.Ala20=
XR_244632.2:n.155G=
NR_156488.1:n.147G=
XM_011532028.2:c.60G= XP_011530330.1:p.Ala20=
NM_000297.4:c.60G= MANE Select NP_000288.1:p.Ala20=
NR_156488.2:n.159G=