Canonical Allele Identifier: CA1474562195
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007843_88007850delinsGCGCCAGC , CM000666.2:g.88007843_88007850delinsGCGCCAGC GRCh38
NC_000004.11:g.88928995_88929002delinsGCGCCAGC , CM000666.1:g.88928995_88929002delinsGCGCCAGC GRCh37
NC_000004.10:g.89148019_89148026delinsGCGCCAGC NCBI36
NG_008604.1:g.5176_5183delinsGCGCCAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.110_117delinsGCGCCAGC MANE Select ENSP00000237596.2:p.Gly37=
ENST00000237596.6:c.110_117delinsGCGCCAGC ENSP00000237596.2:p.Gly37=
NM_000297.3:c.110_117delinsGCGCCAGC NP_000288.1:p.Gly37=
XM_011532028.1:c.110_117delinsGCGCCAGC XP_011530330.1:p.Gly37=
XR_244632.2:n.205_212delinsGCGCCAGC
NR_156488.1:n.197_204delinsGCGCCAGC
XM_011532028.2:c.110_117delinsGCGCCAGC XP_011530330.1:p.Gly37=
NM_000297.4:c.110_117delinsGCGCCAGC MANE Select NP_000288.1:p.Gly37=
NR_156488.2:n.209_216delinsGCGCCAGC
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