Canonical Allele Identifier: CA777985696

Gene: AQP4

Linked Data

• dbSNP Id: rs1260659682
• gnomAD v3: 18-26855461-TTGCCTC-T
• gnomAD v4: 18-26855461-TTGCCTC-T
• MyVariant Identifiers: chr18:g.24435426_24435431del (hg19) ; chr18:g.26855462_26855467del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26855469_26855474del , CM000680.2:g.26855469_26855474del	GRCh38
NC_000018.9:g.24435433_24435438del , CM000680.1:g.24435433_24435438del	GRCh37
NC_000018.8:g.22689431_22689436del	NCBI36
NG_029560.1:g.15286_15291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383168.9:c.*744_*749del MANE Select	ENSP00000372654.4:n.*744_*749del
ENST00000672188.1:c.*744_*749del	ENSP00000500720.1:n.*744_*749del
ENST00000672981.2:c.*657_*662del	ENSP00000500598.2:n.*657_*662del
ENST00000383168.8:c.*744_*749del	ENSP00000372654.4:n.*744_*749del
NM_001650.4:c.*744_*749del	NP_001641.1:n.*744_*749del
NM_004028.3:c.*744_*749del	NP_004019.1:n.*744_*749del
XM_011525942.1:c.*744_*749del	XP_011524244.1:n.*744_*749del
NM_001317384.2:c.*657_*662del	NP_001304313.1:n.*657_*662del
NM_001317387.2:c.*744_*749del	NP_001304316.1:n.*744_*749del
NM_001364286.1:c.*744_*749del	NP_001351215.1:n.*744_*749del
NM_001364287.1:c.*657_*662del	NP_001351216.1:n.*657_*662del
NM_001364289.1:c.*657_*662del	NP_001351218.1:n.*657_*662del
NM_001650.6:c.*744_*749del	NP_001641.1:n.*744_*749del
NM_004028.4:c.*744_*749del	NP_004019.1:n.*744_*749del
XM_011525942.3:c.*744_*749del	XP_011524244.1:n.*744_*749del
NM_001650.7:c.*744_*749del MANE Select	NP_001641.1:n.*744_*749del
NM_001317384.3:c.*657_*662del	NP_001304313.1:n.*657_*662del
NM_001317387.3:c.*744_*749del	NP_001304316.1:n.*744_*749del
NM_001364289.2:c.*657_*662del	NP_001351218.1:n.*657_*662del
NM_004028.5:c.*744_*749del	NP_004019.1:n.*744_*749del