Canonical Allele Identifier: CA1474562121
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007729C= , CM000666.2:g.88007729C= GRCh38
NC_000004.11:g.88928881C= , CM000666.1:g.88928881C= GRCh37
NC_000004.10:g.89147905C= NCBI36
NG_008604.1:g.5062C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-5C= MANE Select ENSP00000237596.2:n.-5C=
ENST00000237596.6:c.-5C= ENSP00000237596.2:n.-5C=
NM_000297.3:c.-5C= NP_000288.1:n.-5C=
XM_011532028.1:c.-5C= XP_011530330.1:n.-5C=
XR_244632.2:n.91C=
NR_156488.1:n.83C=
XM_011532028.2:c.-5C= XP_011530330.1:n.-5C=
NM_000297.4:c.-5C= MANE Select NP_000288.1:n.-5C=
NR_156488.2:n.95C=