Canonical Allele Identifier: CA1474562164
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007792C= , CM000666.2:g.88007792C= GRCh38
NC_000004.11:g.88928944C= , CM000666.1:g.88928944C= GRCh37
NC_000004.10:g.89147968C= NCBI36
NG_008604.1:g.5125C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.59C= MANE Select ENSP00000237596.2:p.Ala20=
ENST00000237596.6:c.59C= ENSP00000237596.2:p.Ala20=
NM_000297.3:c.59C= NP_000288.1:p.Ala20=
XM_011532028.1:c.59C= XP_011530330.1:p.Ala20=
XR_244632.2:n.154C=
NR_156488.1:n.146C=
XM_011532028.2:c.59C= XP_011530330.1:p.Ala20=
NM_000297.4:c.59C= MANE Select NP_000288.1:p.Ala20=
NR_156488.2:n.158C=