Canonical Allele Identifier: CA1474562174
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007807A= , CM000666.2:g.88007807A= GRCh38
NC_000004.11:g.88928959A= , CM000666.1:g.88928959A= GRCh37
NC_000004.10:g.89147983A= NCBI36
NG_008604.1:g.5140A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.74A= MANE Select ENSP00000237596.2:p.Asp25=
ENST00000237596.6:c.74A= ENSP00000237596.2:p.Asp25=
NM_000297.3:c.74A= NP_000288.1:p.Asp25=
XM_011532028.1:c.74A= XP_011530330.1:p.Asp25=
XR_244632.2:n.169A=
NR_156488.1:n.161A=
XM_011532028.2:c.74A= XP_011530330.1:p.Asp25=
NM_000297.4:c.74A= MANE Select NP_000288.1:p.Asp25=
NR_156488.2:n.173A=