Canonical Allele Identifier: CA2291649335

Gene: AQP4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26864919T= , CM000680.2:g.26864919T=	GRCh38
NC_000018.9:g.24444883T= , CM000680.1:g.24444883T=	GRCh37
NC_000018.8:g.22698881T=	NCBI36
NG_029560.1:g.5834A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383168.9:c.32+739A= MANE Select	ENSP00000372654.4:n.32+739A=
ENST00000672188.1:c.32+739A=	ENSP00000500720.1:n.32+739A=
ENST00000672981.2:c.32+739A=	ENSP00000500598.2:n.32+739A=
ENST00000675739.1:c.32+739A=	ENSP00000502364.1:n.32+739A=
ENST00000383168.8:c.32+739A=	ENSP00000372654.4:n.32+739A=
ENST00000383170.3:c.32+739A=	ENSP00000372656.3:n.32+739A=
ENST00000578776.1:c.32+739A=	ENSP00000462075.1:n.32+739A=
ENST00000622234.4:c.32+739A=	ENSP00000484446.1:n.32+739A=
NM_001650.4:c.32+739A=	NP_001641.1:n.32+739A=
NM_001317384.2:c.32+739A=	NP_001304313.1:n.32+739A=
NM_001317387.2:c.32+739A=	NP_001304316.1:n.32+739A=
NM_001364286.1:c.-35+739A=	NP_001351215.1:n.-35+739A=
NM_001364287.1:c.-35+739A=	NP_001351216.1:n.-35+739A=
NM_001650.6:c.32+739A=	NP_001641.1:n.32+739A=
NM_001650.7:c.32+739A= MANE Select	NP_001641.1:n.32+739A=
NM_001317384.3:c.32+739A=	NP_001304313.1:n.32+739A=
NM_001317387.3:c.32+739A=	NP_001304316.1:n.32+739A=