Canonical Allele Identifier: CA3182875305

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22279622A= , CM000673.2:g.22279622A=	GRCh38
NC_000011.9:g.22301168A= , CM000673.1:g.22301168A=	GRCh37
NC_000011.8:g.22257744A=	NCBI36
NG_015844.1:g.91447A= , LRG_868:g.91447A=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.2599A= MANE Select	NP_998764.1:p.Arg867=
ENST00000324559.9:c.2599A= MANE Select	ENSP00000315371.9:p.Arg867=
NM_001142649.1:c.2596A=	NP_001136121.1:p.Arg866=
NM_001142649.2:c.2596A=	NP_001136121.1:p.Arg866=
NM_213599.2:c.2599A= , LRG_868t1:c.2599A=	NP_998764.1:p.Arg867=
ENST00000324559.8:c.2599A=	ENSP00000315371.8:p.Arg867=
ENST00000648804.1:n.2934A=
ENST00000682266.1:c.2149A=	ENSP00000507766.1:p.Arg717=
ENST00000682341.1:c.2557A=	ENSP00000508251.1:p.Arg853=
ENST00000683197.1:c.*63A=	ENSP00000507641.1:n.*63A=
ENST00000683411.1:c.2149A=	ENSP00000508397.1:p.Arg717=
ENST00000683437.1:c.2149A=	ENSP00000508408.1:p.Arg717=
ENST00000683613.1:n.3593A=
ENST00000684663.1:c.2554A=	ENSP00000508009.1:p.Arg852=
XM_005252820.2:c.2557A=	XP_005252877.2:p.Arg853=
XM_005252820.3:c.2557A=	XP_005252877.2:p.Arg853=
XM_005252821.2:c.2554A=	XP_005252878.2:p.Arg852=
XM_005252821.3:c.2554A=	XP_005252878.2:p.Arg852=
XM_005252822.3:c.2521A=	XP_005252879.1:p.Arg841=
XM_005252822.4:c.2521A=	XP_005252879.1:p.Arg841=
XM_005252823.3:c.2518A=	XP_005252880.1:p.Arg840=
XM_011519949.1:c.2506A=	XP_011518251.1:p.Arg836=
XM_011519949.2:c.2506A=	XP_011518251.1:p.Arg836=