Canonical Allele Identifier: CA1474562178
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007811G= , CM000666.2:g.88007811G= GRCh38
NC_000004.11:g.88928963G= , CM000666.1:g.88928963G= GRCh37
NC_000004.10:g.89147987G= NCBI36
NG_008604.1:g.5144G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.78G= MANE Select ENSP00000237596.2:p.Pro26=
ENST00000237596.6:c.78G= ENSP00000237596.2:p.Pro26=
NM_000297.3:c.78G= NP_000288.1:p.Pro26=
XM_011532028.1:c.78G= XP_011530330.1:p.Pro26=
XR_244632.2:n.173G=
NR_156488.1:n.165G=
XM_011532028.2:c.78G= XP_011530330.1:p.Pro26=
NM_000297.4:c.78G= MANE Select NP_000288.1:p.Pro26=
NR_156488.2:n.177G=