Canonical Allele Identifier: CA1957413608

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250793T= , CM000673.2:g.22250793T=	GRCh38
NC_000011.9:g.22272339T= , CM000673.1:g.22272339T=	GRCh37
NC_000011.8:g.22228915T=	NCBI36
NG_015844.1:g.62618T= , LRG_868:g.62618T=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1066T= MANE Select	NP_998764.1:p.Cys356=
ENST00000324559.9:c.1066T= MANE Select	ENSP00000315371.9:p.Cys356=
NM_001142649.1:c.1063T=	NP_001136121.1:p.Cys355=
NM_001142649.2:c.1063T=	NP_001136121.1:p.Cys355=
NM_213599.2:c.1066T= , LRG_868t1:c.1066T=	NP_998764.1:p.Cys356=
ENST00000324559.8:c.1066T=	ENSP00000315371.8:p.Cys356=
ENST00000648804.1:n.1401T=
ENST00000682089.1:n.386T=
ENST00000682266.1:c.616T=	ENSP00000507766.1:p.Cys206=
ENST00000682341.1:c.1024T=	ENSP00000508251.1:p.Cys342=
ENST00000682530.1:c.*998T=	ENSP00000506805.1:n.*998T=
ENST00000683197.1:c.1024T=	ENSP00000507641.1:p.Cys342=
ENST00000683411.1:c.616T=	ENSP00000508397.1:p.Cys206=
ENST00000683437.1:c.616T=	ENSP00000508408.1:p.Cys206=
ENST00000683613.1:n.2060T=
ENST00000683834.1:n.1266T=
ENST00000684663.1:c.1021T=	ENSP00000508009.1:p.Cys341=
XM_005252820.2:c.1024T=	XP_005252877.2:p.Cys342=
XM_005252820.3:c.1024T=	XP_005252877.2:p.Cys342=
XM_005252821.2:c.1021T=	XP_005252878.2:p.Cys341=
XM_005252821.3:c.1021T=	XP_005252878.2:p.Cys341=
XM_005252822.3:c.988T=	XP_005252879.1:p.Cys330=
XM_005252822.4:c.988T=	XP_005252879.1:p.Cys330=
XM_005252823.3:c.985T=	XP_005252880.1:p.Cys329=
XM_011519949.1:c.973T=	XP_011518251.1:p.Cys325=
XM_011519949.2:c.973T=	XP_011518251.1:p.Cys325=