Canonical Allele Identifier: CA2291645265

Gene: AQP4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26855597A= , CM000680.2:g.26855597A=	GRCh38
NC_000018.9:g.24435561A= , CM000680.1:g.24435561A=	GRCh37
NC_000018.8:g.22689559A=	NCBI36
NG_029560.1:g.15156T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383168.9:c.*614T= MANE Select	ENSP00000372654.4:n.*614T=
ENST00000672188.1:c.*614T=	ENSP00000500720.1:n.*614T=
ENST00000672981.2:c.*527T=	ENSP00000500598.2:n.*527T=
ENST00000383168.8:c.*614T=	ENSP00000372654.4:n.*614T=
NM_001650.4:c.*614T=	NP_001641.1:n.*614T=
NM_004028.3:c.*614T=	NP_004019.1:n.*614T=
XM_011525942.1:c.*614T=	XP_011524244.1:n.*614T=
NM_001317384.2:c.*527T=	NP_001304313.1:n.*527T=
NM_001317387.2:c.*614T=	NP_001304316.1:n.*614T=
NM_001364286.1:c.*614T=	NP_001351215.1:n.*614T=
NM_001364287.1:c.*527T=	NP_001351216.1:n.*527T=
NM_001364289.1:c.*527T=	NP_001351218.1:n.*527T=
NM_001650.6:c.*614T=	NP_001641.1:n.*614T=
NM_004028.4:c.*614T=	NP_004019.1:n.*614T=
XM_011525942.3:c.*614T=	XP_011524244.1:n.*614T=
NM_001650.7:c.*614T= MANE Select	NP_001641.1:n.*614T=
NM_001317384.3:c.*527T=	NP_001304313.1:n.*527T=
NM_001317387.3:c.*614T=	NP_001304316.1:n.*614T=
NM_001364289.2:c.*527T=	NP_001351218.1:n.*527T=
NM_004028.5:c.*614T=	NP_004019.1:n.*614T=