Canonical Allele Identifier: CA2035390385
Gene: AQP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49950918_49950941delinsTCTGCCCTCAACTGGCCACAGGCC , CM000674.2:g.49950918_49950941delinsTCTGCCCTCAACTGGCCACAGGCC GRCh38
NC_000012.11:g.50344701_50344724delinsTCTGCCCTCAACTGGCCACAGGCC , CM000674.1:g.50344701_50344724delinsTCTGCCCTCAACTGGCCACAGGCC GRCh37
NC_000012.10:g.48630968_48630991delinsTCTGCCCTCAACTGGCCACAGGCC NCBI36
NG_008913.1:g.5178_5201delinsTCTGCCCTCAACTGGCCACAGGCC , LRG_717:g.5178_5201delinsTCTGCCCTCAACTGGCCACAGGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000199280.4:c.88_111delinsTCTGCCCTCAACTGGCCACAGGCC MANE Select ENSP00000199280.3:p.Ser30=
ENST00000199280.3:c.88_111delinsTCTGCCCTCAACTGGCCACAGGCC ENSP00000199280.3:p.Ser30=
ENST00000550862.1:c.88_111delinsTCTGCCCTCAACTGGCCACAGGCC ENSP00000450022.1:p.Ser30=
ENST00000551526.5:c.88_111delinsTCTGCCCTCAACTGGCCACAGGCC ENSP00000447148.1:p.Ser30=
NM_000486.5:c.88_111delinsTCTGCCCTCAACTGGCCACAGGCC , LRG_717t1:c.88_111delinsTCTGCCCTCAACTGGCCACAGGCC NP_000477.1:p.Ser30=
NM_000486.6:c.88_111delinsTCTGCCCTCAACTGGCCACAGGCC MANE Select NP_000477.1:p.Ser30=