Canonical Allele Identifier: CA1474562219
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007888T= , CM000666.2:g.88007888T= GRCh38
NC_000004.11:g.88929040T= , CM000666.1:g.88929040T= GRCh37
NC_000004.10:g.89148064T= NCBI36
NG_008604.1:g.5221T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.155T= MANE Select ENSP00000237596.2:p.Leu52=
ENST00000237596.6:c.155T= ENSP00000237596.2:p.Leu52=
NM_000297.3:c.155T= NP_000288.1:p.Leu52=
XM_011532028.1:c.155T= XP_011530330.1:p.Leu52=
XR_244632.2:n.250T=
NR_156488.1:n.242T=
XM_011532028.2:c.155T= XP_011530330.1:p.Leu52=
NM_000297.4:c.155T= MANE Select NP_000288.1:p.Leu52=
NR_156488.2:n.254T=