Canonical Allele Identifier: CA1957419843

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262214C= , CM000673.2:g.22262214C=	GRCh38
NC_000011.9:g.22283760C= , CM000673.1:g.22283760C=	GRCh37
NC_000011.8:g.22240336C=	NCBI36
NG_015844.1:g.74039C= , LRG_868:g.74039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1266C=	ENSP00000507766.1:p.Cys422=
ENST00000682341.1:c.1674C=	ENSP00000508251.1:p.Cys558=
ENST00000683197.1:c.1674C=	ENSP00000507641.1:p.Cys558=
ENST00000683411.1:c.1266C=	ENSP00000508397.1:p.Cys422=
ENST00000683437.1:c.1266C=	ENSP00000508408.1:p.Cys422=
ENST00000683613.1:n.2710C=
ENST00000684663.1:c.1671C=	ENSP00000508009.1:p.Cys557=
ENST00000324559.9:c.1716C= MANE Select	ENSP00000315371.9:p.Cys572=
ENST00000648804.1:n.2051C=
ENST00000324559.8:c.1716C=	ENSP00000315371.8:p.Cys572=
NM_001142649.1:c.1713C=	NP_001136121.1:p.Cys571=
NM_213599.2:c.1716C= , LRG_868t1:c.1716C=	NP_998764.1:p.Cys572=
XM_005252820.2:c.1674C=	XP_005252877.2:p.Cys558=
XM_005252821.2:c.1671C=	XP_005252878.2:p.Cys557=
XM_005252822.3:c.1638C=	XP_005252879.1:p.Cys546=
XM_005252823.3:c.1635C=	XP_005252880.1:p.Cys545=
XM_011519949.1:c.1623C=	XP_011518251.1:p.Cys541=
XM_005252820.3:c.1674C=	XP_005252877.2:p.Cys558=
XM_005252821.3:c.1671C=	XP_005252878.2:p.Cys557=
XM_005252822.4:c.1638C=	XP_005252879.1:p.Cys546=
XM_011519949.2:c.1623C=	XP_011518251.1:p.Cys541=
NM_001142649.2:c.1713C=	NP_001136121.1:p.Cys571=
NM_213599.3:c.1716C= MANE Select	NP_998764.1:p.Cys572=