Canonical Allele Identifier: CA1474579605
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88046791A= , CM000666.2:g.88046791A= GRCh38
NC_000004.11:g.88967943A= , CM000666.1:g.88967943A= GRCh37
NC_000004.10:g.89186967A= NCBI36
NG_008604.1:g.44124A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1469A= MANE Select ENSP00000237596.2:p.Glu490=
ENST00000237596.6:c.1469A= ENSP00000237596.2:p.Glu490=
ENST00000508588.5:c.-199+3334A= ENSP00000427131.1:n.-199+3334A=
NM_000297.3:c.1469A= NP_000288.1:p.Glu490=
XM_011532028.1:c.1244A= XP_011530330.1:p.Glu415=
XM_011532029.1:c.749A= XP_011530331.1:p.Glu250=
XM_011532030.1:c.629A= XP_011530332.1:p.Glu210=
XR_244632.2:n.1564A=
NR_156488.1:n.1556A=
XM_011532028.2:c.1244A= XP_011530330.1:p.Glu415=
XM_011532030.2:c.629A= XP_011530332.1:p.Glu210=
NM_000297.4:c.1469A= MANE Select NP_000288.1:p.Glu490=
NR_156488.2:n.1568A=