Canonical Allele Identifier: CA1957407927

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22236308C= , CM000673.2:g.22236308C=	GRCh38
NC_000011.9:g.22257854C= , CM000673.1:g.22257854C=	GRCh37
NC_000011.8:g.22214430C=	NCBI36
NG_015844.1:g.48133C= , LRG_868:g.48133C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.312+32C=	ENSP00000507766.1:n.312+32C=
ENST00000682341.1:c.720+32C=	ENSP00000508251.1:n.720+32C=
ENST00000682530.1:c.*694+32C=	ENSP00000506805.1:n.*694+32C=
ENST00000682684.1:n.1141+32C=
ENST00000683197.1:c.720+32C=	ENSP00000507641.1:n.720+32C=
ENST00000683411.1:c.312+32C=	ENSP00000508397.1:n.312+32C=
ENST00000683437.1:c.312+32C=	ENSP00000508408.1:n.312+32C=
ENST00000683613.1:n.1756+32C=
ENST00000683834.1:n.962+32C=
ENST00000684663.1:c.717+32C=	ENSP00000508009.1:n.717+32C=
ENST00000324559.9:c.762+32C= MANE Select	ENSP00000315371.9:n.762+32C=
ENST00000648804.1:n.1213+8722C=
ENST00000324559.8:c.762+32C=	ENSP00000315371.8:n.762+32C=
NM_001142649.1:c.759+32C=	NP_001136121.1:n.759+32C=
NM_213599.2:c.762+32C= , LRG_868t1:c.762+32C=	NP_998764.1:n.762+32C=
XM_005252820.2:c.720+32C=	XP_005252877.2:n.720+32C=
XM_005252821.2:c.717+32C=	XP_005252878.2:n.717+32C=
XM_005252822.3:c.684+32C=	XP_005252879.1:n.684+32C=
XM_005252823.3:c.681+32C=	XP_005252880.1:n.681+32C=
XM_011519949.1:c.669+32C=	XP_011518251.1:n.669+32C=
XM_005252820.3:c.720+32C=	XP_005252877.2:n.720+32C=
XM_005252821.3:c.717+32C=	XP_005252878.2:n.717+32C=
XM_005252822.4:c.684+32C=	XP_005252879.1:n.684+32C=
XM_011519949.2:c.669+32C=	XP_011518251.1:n.669+32C=
NM_001142649.2:c.759+32C=	NP_001136121.1:n.759+32C=
NM_213599.3:c.762+32C= MANE Select	NP_998764.1:n.762+32C=