Canonical Allele Identifier: CA2291645249

Gene: AQP4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26855573C= , CM000680.2:g.26855573C=	GRCh38
NC_000018.9:g.24435537C= , CM000680.1:g.24435537C=	GRCh37
NC_000018.8:g.22689535C=	NCBI36
NG_029560.1:g.15180G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383168.9:c.*638G= MANE Select	ENSP00000372654.4:n.*638G=
ENST00000672188.1:c.*638G=	ENSP00000500720.1:n.*638G=
ENST00000672981.2:c.*551G=	ENSP00000500598.2:n.*551G=
ENST00000383168.8:c.*638G=	ENSP00000372654.4:n.*638G=
NM_001650.4:c.*638G=	NP_001641.1:n.*638G=
NM_004028.3:c.*638G=	NP_004019.1:n.*638G=
XM_011525942.1:c.*638G=	XP_011524244.1:n.*638G=
NM_001317384.2:c.*551G=	NP_001304313.1:n.*551G=
NM_001317387.2:c.*638G=	NP_001304316.1:n.*638G=
NM_001364286.1:c.*638G=	NP_001351215.1:n.*638G=
NM_001364287.1:c.*551G=	NP_001351216.1:n.*551G=
NM_001364289.1:c.*551G=	NP_001351218.1:n.*551G=
NM_001650.6:c.*638G=	NP_001641.1:n.*638G=
NM_004028.4:c.*638G=	NP_004019.1:n.*638G=
XM_011525942.3:c.*638G=	XP_011524244.1:n.*638G=
NM_001650.7:c.*638G= MANE Select	NP_001641.1:n.*638G=
NM_001317384.3:c.*551G=	NP_001304313.1:n.*551G=
NM_001317387.3:c.*638G=	NP_001304316.1:n.*638G=
NM_001364289.2:c.*551G=	NP_001351218.1:n.*551G=
NM_004028.5:c.*638G=	NP_004019.1:n.*638G=