Canonical Allele Identifier: CA1474562359
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008148_88008149delinsCG , CM000666.2:g.88008148_88008149delinsCG GRCh38
NC_000004.11:g.88929300_88929301delinsCG , CM000666.1:g.88929300_88929301delinsCG GRCh37
NC_000004.10:g.89148324_89148325delinsCG NCBI36
NG_008604.1:g.5481_5482delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.415_416delinsCG MANE Select ENSP00000237596.2:p.Arg139=
ENST00000237596.6:c.415_416delinsCG ENSP00000237596.2:p.Arg139=
NM_000297.3:c.415_416delinsCG NP_000288.1:p.Arg139=
XM_011532028.1:c.415_416delinsCG XP_011530330.1:p.Arg139=
XR_244632.2:n.510_511delinsCG
NR_156488.1:n.502_503delinsCG
XM_011532028.2:c.415_416delinsCG XP_011530330.1:p.Arg139=
NM_000297.4:c.415_416delinsCG MANE Select NP_000288.1:p.Arg139=
NR_156488.2:n.514_515delinsCG