Canonical Allele Identifier: CA1474578045
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88043250A= , CM000666.2:g.88043250A= GRCh38
NC_000004.11:g.88964402A= , CM000666.1:g.88964402A= GRCh37
NC_000004.10:g.89183426A= NCBI36
NG_008604.1:g.40583A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1112A= MANE Select ENSP00000237596.2:p.Glu371=
ENST00000237596.6:c.1112A= ENSP00000237596.2:p.Glu371=
ENST00000506367.1:n.559A=
NM_000297.3:c.1112A= NP_000288.1:p.Glu371=
XM_011532028.1:c.1095-3392A= XP_011530330.1:n.1095-3392A=
XM_011532029.1:c.392A= XP_011530331.1:p.Glu131=
XM_011532030.1:c.272A= XP_011530332.1:p.Glu91=
XR_244632.2:n.1207A=
NR_156488.1:n.1199A=
XM_011532028.2:c.1095-3392A= XP_011530330.1:n.1095-3392A=
XM_011532030.2:c.272A= XP_011530332.1:p.Glu91=
NM_000297.4:c.1112A= MANE Select NP_000288.1:p.Glu371=
NR_156488.2:n.1211A=