Canonical Allele Identifier: CA1957403007

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272914A= , CM000673.2:g.22272914A=	GRCh38
NC_000011.9:g.22294460A= , CM000673.1:g.22294460A=	GRCh37
NC_000011.8:g.22251036A=	NCBI36
NG_015844.1:g.84739A= , LRG_868:g.84739A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.177A=
ENST00000682266.1:c.1710A=	ENSP00000507766.1:p.Val570=
ENST00000682341.1:c.2118A=	ENSP00000508251.1:p.Val706=
ENST00000683197.1:c.2118A=	ENSP00000507641.1:p.Val706=
ENST00000683411.1:c.1710A=	ENSP00000508397.1:p.Val570=
ENST00000683437.1:c.1710A=	ENSP00000508408.1:p.Val570=
ENST00000683613.1:n.3154A=
ENST00000684663.1:c.2115A=	ENSP00000508009.1:p.Val705=
ENST00000324559.9:c.2160A= MANE Select	ENSP00000315371.9:p.Val720=
ENST00000648804.1:n.2495A=
ENST00000324559.8:c.2160A=	ENSP00000315371.8:p.Val720=
ENST00000532043.1:n.177A=
NM_001142649.1:c.2157A=	NP_001136121.1:p.Val719=
NM_213599.2:c.2160A= , LRG_868t1:c.2160A=	NP_998764.1:p.Val720=
XM_005252820.2:c.2118A=	XP_005252877.2:p.Val706=
XM_005252821.2:c.2115A=	XP_005252878.2:p.Val705=
XM_005252822.3:c.2082A=	XP_005252879.1:p.Val694=
XM_005252823.3:c.2079A=	XP_005252880.1:p.Val693=
XM_011519949.1:c.2067A=	XP_011518251.1:p.Val689=
XM_005252820.3:c.2118A=	XP_005252877.2:p.Val706=
XM_005252821.3:c.2115A=	XP_005252878.2:p.Val705=
XM_005252822.4:c.2082A=	XP_005252879.1:p.Val694=
XM_011519949.2:c.2067A=	XP_011518251.1:p.Val689=
NM_001142649.2:c.2157A=	NP_001136121.1:p.Val719=
NM_213599.3:c.2160A= MANE Select	NP_998764.1:p.Val720=