Canonical Allele Identifier: CA1474562085
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007695C= , CM000666.2:g.88007695C= GRCh38
NC_000004.11:g.88928847C= , CM000666.1:g.88928847C= GRCh37
NC_000004.10:g.89147871C= NCBI36
NG_008604.1:g.5028C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-39C= MANE Select ENSP00000237596.2:n.-39C=
ENST00000237596.6:c.-39C= ENSP00000237596.2:n.-39C=
NM_000297.3:c.-39C= NP_000288.1:n.-39C=
XM_011532028.1:c.-39C= XP_011530330.1:n.-39C=
XR_244632.2:n.57C=
NR_156488.1:n.49C=
XM_011532028.2:c.-39C= XP_011530330.1:n.-39C=
NM_000297.4:c.-39C= MANE Select NP_000288.1:n.-39C=
NR_156488.2:n.61C=
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