Canonical Allele Identifier: CA1474562341
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008119C= , CM000666.2:g.88008119C= GRCh38
NC_000004.11:g.88929271C= , CM000666.1:g.88929271C= GRCh37
NC_000004.10:g.89148295C= NCBI36
NG_008604.1:g.5452C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.386C= MANE Select ENSP00000237596.2:p.Ser129=
ENST00000237596.6:c.386C= ENSP00000237596.2:p.Ser129=
NM_000297.3:c.386C= NP_000288.1:p.Ser129=
XM_011532028.1:c.386C= XP_011530330.1:p.Ser129=
XR_244632.2:n.481C=
NR_156488.1:n.473C=
XM_011532028.2:c.386C= XP_011530330.1:p.Ser129=
NM_000297.4:c.386C= MANE Select NP_000288.1:p.Ser129=
NR_156488.2:n.485C=