Canonical Allele Identifier: CA2291645181
Gene: AQP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.26855438_26855439delinsGT , CM000680.2:g.26855438_26855439delinsGT GRCh38
NC_000018.9:g.24435402_24435403delinsGT , CM000680.1:g.24435402_24435403delinsGT GRCh37
NC_000018.8:g.22689400_22689401delinsGT NCBI36
NG_029560.1:g.15314_15315delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000383168.9:c.*772_*773delinsAC MANE Select ENSP00000372654.4:n.*772_*773delinsAC
ENST00000672188.1:c.*772_*773delinsAC ENSP00000500720.1:n.*772_*773delinsAC
ENST00000672981.2:c.*685_*686delinsAC ENSP00000500598.2:n.*685_*686delinsAC
ENST00000383168.8:c.*772_*773delinsAC ENSP00000372654.4:n.*772_*773delinsAC
NM_001650.4:c.*772_*773delinsAC NP_001641.1:n.*772_*773delinsAC
NM_004028.3:c.*772_*773delinsAC NP_004019.1:n.*772_*773delinsAC
XM_011525942.1:c.*772_*773delinsAC XP_011524244.1:n.*772_*773delinsAC
NM_001317384.2:c.*685_*686delinsAC NP_001304313.1:n.*685_*686delinsAC
NM_001317387.2:c.*772_*773delinsAC NP_001304316.1:n.*772_*773delinsAC
NM_001364286.1:c.*772_*773delinsAC NP_001351215.1:n.*772_*773delinsAC
NM_001364287.1:c.*685_*686delinsAC NP_001351216.1:n.*685_*686delinsAC
NM_001364289.1:c.*685_*686delinsAC NP_001351218.1:n.*685_*686delinsAC
NM_001650.6:c.*772_*773delinsAC NP_001641.1:n.*772_*773delinsAC
NM_004028.4:c.*772_*773delinsAC NP_004019.1:n.*772_*773delinsAC
XM_011525942.3:c.*772_*773delinsAC XP_011524244.1:n.*772_*773delinsAC
NM_001650.7:c.*772_*773delinsAC MANE Select NP_001641.1:n.*772_*773delinsAC
NM_001317384.3:c.*685_*686delinsAC NP_001304313.1:n.*685_*686delinsAC
NM_001317387.3:c.*772_*773delinsAC NP_001304316.1:n.*772_*773delinsAC
NM_001364289.2:c.*685_*686delinsAC NP_001351218.1:n.*685_*686delinsAC
NM_004028.5:c.*772_*773delinsAC NP_004019.1:n.*772_*773delinsAC