Canonical Allele Identifier: CA3183114521

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22225988G= , CM000673.2:g.22225988G=	GRCh38
NC_000011.9:g.22247534G= , CM000673.1:g.22247534G=	GRCh37
NC_000011.8:g.22204110G=	NCBI36
NG_015844.1:g.37813G= , LRG_868:g.37813G=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.299G= MANE Select	NP_998764.1:p.Arg100=
ENST00000324559.9:c.299G= MANE Select	ENSP00000315371.9:p.Arg100=
NM_001142649.1:c.296G=	NP_001136121.1:p.Arg99=
NM_001142649.2:c.296G=	NP_001136121.1:p.Arg99=
NM_213599.2:c.299G= , LRG_868t1:c.299G=	NP_998764.1:p.Arg100=
ENST00000324559.8:c.299G=	ENSP00000315371.8:p.Arg100=
ENST00000648804.1:n.864G=
ENST00000682266.1:c.-152G=	ENSP00000507766.1:n.-152G=
ENST00000682341.1:c.257G=	ENSP00000508251.1:p.Arg86=
ENST00000682530.1:c.*231G=	ENSP00000506805.1:n.*231G=
ENST00000682684.1:n.678G=
ENST00000683197.1:c.257G=	ENSP00000507641.1:p.Arg86=
ENST00000683411.1:c.-152G=	ENSP00000508397.1:n.-152G=
ENST00000683437.1:c.-152G=	ENSP00000508408.1:n.-152G=
ENST00000683613.1:n.1293G=
ENST00000683834.1:n.499G=
ENST00000684663.1:c.254G=	ENSP00000508009.1:p.Arg85=
XM_005252820.2:c.257G=	XP_005252877.2:p.Arg86=
XM_005252820.3:c.257G=	XP_005252877.2:p.Arg86=
XM_005252821.2:c.254G=	XP_005252878.2:p.Arg85=
XM_005252821.3:c.254G=	XP_005252878.2:p.Arg85=
XM_005252822.3:c.221G=	XP_005252879.1:p.Arg74=
XM_005252822.4:c.221G=	XP_005252879.1:p.Arg74=
XM_005252823.3:c.218G=	XP_005252880.1:p.Arg73=
XM_011519949.1:c.206G=	XP_011518251.1:p.Arg69=
XM_011519949.2:c.206G=	XP_011518251.1:p.Arg69=