Canonical Allele Identifier: CA1957416915

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255397C= , CM000673.2:g.22255397C=	GRCh38
NC_000011.9:g.22276943C= , CM000673.1:g.22276943C=	GRCh37
NC_000011.8:g.22233519C=	NCBI36
NG_015844.1:g.67222C= , LRG_868:g.67222C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.527C=
ENST00000682266.1:c.757C=	ENSP00000507766.1:p.Gln253=
ENST00000682341.1:c.1165C=	ENSP00000508251.1:p.Gln389=
ENST00000682530.1:c.*1139C=	ENSP00000506805.1:n.*1139C=
ENST00000683197.1:c.1165C=	ENSP00000507641.1:p.Gln389=
ENST00000683411.1:c.757C=	ENSP00000508397.1:p.Gln253=
ENST00000683437.1:c.757C=	ENSP00000508408.1:p.Gln253=
ENST00000683613.1:n.2201C=
ENST00000683834.1:n.1407C=
ENST00000684663.1:c.1162C=	ENSP00000508009.1:p.Gln388=
ENST00000324559.9:c.1207C= MANE Select	ENSP00000315371.9:p.Gln403=
ENST00000648804.1:n.1542C=
ENST00000324559.8:c.1207C=	ENSP00000315371.8:p.Gln403=
NM_001142649.1:c.1204C=	NP_001136121.1:p.Gln402=
NM_213599.2:c.1207C= , LRG_868t1:c.1207C=	NP_998764.1:p.Gln403=
XM_005252820.2:c.1165C=	XP_005252877.2:p.Gln389=
XM_005252821.2:c.1162C=	XP_005252878.2:p.Gln388=
XM_005252822.3:c.1129C=	XP_005252879.1:p.Gln377=
XM_005252823.3:c.1126C=	XP_005252880.1:p.Gln376=
XM_011519949.1:c.1114C=	XP_011518251.1:p.Gln372=
XM_005252820.3:c.1165C=	XP_005252877.2:p.Gln389=
XM_005252821.3:c.1162C=	XP_005252878.2:p.Gln388=
XM_005252822.4:c.1129C=	XP_005252879.1:p.Gln377=
XM_011519949.2:c.1114C=	XP_011518251.1:p.Gln372=
NM_001142649.2:c.1204C=	NP_001136121.1:p.Gln402=
NM_213599.3:c.1207C= MANE Select	NP_998764.1:p.Gln403=