Canonical Allele Identifier: CA1957407901

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22236286G= , CM000673.2:g.22236286G=	GRCh38
NC_000011.9:g.22257832G= , CM000673.1:g.22257832G=	GRCh37
NC_000011.8:g.22214408G=	NCBI36
NG_015844.1:g.48111G= , LRG_868:g.48111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.312+10G=	ENSP00000507766.1:n.312+10G=
ENST00000682341.1:c.720+10G=	ENSP00000508251.1:n.720+10G=
ENST00000682530.1:c.*694+10G=	ENSP00000506805.1:n.*694+10G=
ENST00000682684.1:n.1141+10G=
ENST00000683197.1:c.720+10G=	ENSP00000507641.1:n.720+10G=
ENST00000683411.1:c.312+10G=	ENSP00000508397.1:n.312+10G=
ENST00000683437.1:c.312+10G=	ENSP00000508408.1:n.312+10G=
ENST00000683613.1:n.1756+10G=
ENST00000683834.1:n.962+10G=
ENST00000684663.1:c.717+10G=	ENSP00000508009.1:n.717+10G=
ENST00000324559.9:c.762+10G= MANE Select	ENSP00000315371.9:n.762+10G=
ENST00000648804.1:n.1213+8700G=
ENST00000324559.8:c.762+10G=	ENSP00000315371.8:n.762+10G=
NM_001142649.1:c.759+10G=	NP_001136121.1:n.759+10G=
NM_213599.2:c.762+10G= , LRG_868t1:c.762+10G=	NP_998764.1:n.762+10G=
XM_005252820.2:c.720+10G=	XP_005252877.2:n.720+10G=
XM_005252821.2:c.717+10G=	XP_005252878.2:n.717+10G=
XM_005252822.3:c.684+10G=	XP_005252879.1:n.684+10G=
XM_005252823.3:c.681+10G=	XP_005252880.1:n.681+10G=
XM_011519949.1:c.669+10G=	XP_011518251.1:n.669+10G=
XM_005252820.3:c.720+10G=	XP_005252877.2:n.720+10G=
XM_005252821.3:c.717+10G=	XP_005252878.2:n.717+10G=
XM_005252822.4:c.684+10G=	XP_005252879.1:n.684+10G=
XM_011519949.2:c.669+10G=	XP_011518251.1:n.669+10G=
NM_001142649.2:c.759+10G=	NP_001136121.1:n.759+10G=
NM_213599.3:c.762+10G= MANE Select	NP_998764.1:n.762+10G=