Canonical Allele Identifier: CA1957420190

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262967A= , CM000673.2:g.22262967A=	GRCh38
NC_000011.9:g.22284513A= , CM000673.1:g.22284513A=	GRCh37
NC_000011.8:g.22241089A=	NCBI36
NG_015844.1:g.74792A= , LRG_868:g.74792A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1372A=	ENSP00000507766.1:p.Ile458=
ENST00000682341.1:c.1780A=	ENSP00000508251.1:p.Ile594=
ENST00000683197.1:c.1780A=	ENSP00000507641.1:p.Ile594=
ENST00000683411.1:c.1372A=	ENSP00000508397.1:p.Ile458=
ENST00000683437.1:c.1372A=	ENSP00000508408.1:p.Ile458=
ENST00000683613.1:n.2816A=
ENST00000684663.1:c.1777A=	ENSP00000508009.1:p.Ile593=
ENST00000324559.9:c.1822A= MANE Select	ENSP00000315371.9:p.Ile608=
ENST00000648804.1:n.2157A=
ENST00000324559.8:c.1822A=	ENSP00000315371.8:p.Ile608=
NM_001142649.1:c.1819A=	NP_001136121.1:p.Ile607=
NM_213599.2:c.1822A= , LRG_868t1:c.1822A=	NP_998764.1:p.Ile608=
XM_005252820.2:c.1780A=	XP_005252877.2:p.Ile594=
XM_005252821.2:c.1777A=	XP_005252878.2:p.Ile593=
XM_005252822.3:c.1744A=	XP_005252879.1:p.Ile582=
XM_005252823.3:c.1741A=	XP_005252880.1:p.Ile581=
XM_011519949.1:c.1729A=	XP_011518251.1:p.Ile577=
XM_005252820.3:c.1780A=	XP_005252877.2:p.Ile594=
XM_005252821.3:c.1777A=	XP_005252878.2:p.Ile593=
XM_005252822.4:c.1744A=	XP_005252879.1:p.Ile582=
XM_011519949.2:c.1729A=	XP_011518251.1:p.Ile577=
NM_001142649.2:c.1819A=	NP_001136121.1:p.Ile607=
NM_213599.3:c.1822A= MANE Select	NP_998764.1:p.Ile608=