Canonical Allele Identifier: CA1957413160

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250247G= , CM000673.2:g.22250247G=	GRCh38
NC_000011.9:g.22271793G= , CM000673.1:g.22271793G=	GRCh37
NC_000011.8:g.22228369G=	NCBI36
NG_015844.1:g.62072G= , LRG_868:g.62072G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.209G=
ENST00000682266.1:c.439G=	ENSP00000507766.1:p.Gly147=
ENST00000682341.1:c.847G=	ENSP00000508251.1:p.Gly283=
ENST00000682530.1:c.*821G=	ENSP00000506805.1:n.*821G=
ENST00000683197.1:c.847G=	ENSP00000507641.1:p.Gly283=
ENST00000683411.1:c.439G=	ENSP00000508397.1:p.Gly147=
ENST00000683437.1:c.439G=	ENSP00000508408.1:p.Gly147=
ENST00000683613.1:n.1883G=
ENST00000683834.1:n.1089G=
ENST00000684663.1:c.844G=	ENSP00000508009.1:p.Gly282=
ENST00000324559.9:c.889G= MANE Select	ENSP00000315371.9:p.Gly297=
ENST00000648804.1:n.1224G=
ENST00000324559.8:c.889G=	ENSP00000315371.8:p.Gly297=
NM_001142649.1:c.886G=	NP_001136121.1:p.Gly296=
NM_213599.2:c.889G= , LRG_868t1:c.889G=	NP_998764.1:p.Gly297=
XM_005252820.2:c.847G=	XP_005252877.2:p.Gly283=
XM_005252821.2:c.844G=	XP_005252878.2:p.Gly282=
XM_005252822.3:c.811G=	XP_005252879.1:p.Gly271=
XM_005252823.3:c.808G=	XP_005252880.1:p.Gly270=
XM_011519949.1:c.796G=	XP_011518251.1:p.Gly266=
XM_005252820.3:c.847G=	XP_005252877.2:p.Gly283=
XM_005252821.3:c.844G=	XP_005252878.2:p.Gly282=
XM_005252822.4:c.811G=	XP_005252879.1:p.Gly271=
XM_011519949.2:c.796G=	XP_011518251.1:p.Gly266=
NM_001142649.2:c.886G=	NP_001136121.1:p.Gly296=
NM_213599.3:c.889G= MANE Select	NP_998764.1:p.Gly297=