Canonical Allele Identifier: CA1957420185

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262948T= , CM000673.2:g.22262948T=	GRCh38
NC_000011.9:g.22284494T= , CM000673.1:g.22284494T=	GRCh37
NC_000011.8:g.22241070T=	NCBI36
NG_015844.1:g.74773T= , LRG_868:g.74773T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1353T=	ENSP00000507766.1:p.Cys451=
ENST00000682341.1:c.1761T=	ENSP00000508251.1:p.Cys587=
ENST00000683197.1:c.1761T=	ENSP00000507641.1:p.Cys587=
ENST00000683411.1:c.1353T=	ENSP00000508397.1:p.Cys451=
ENST00000683437.1:c.1353T=	ENSP00000508408.1:p.Cys451=
ENST00000683613.1:n.2797T=
ENST00000684663.1:c.1758T=	ENSP00000508009.1:p.Cys586=
ENST00000324559.9:c.1803T= MANE Select	ENSP00000315371.9:p.Cys601=
ENST00000648804.1:n.2138T=
ENST00000324559.8:c.1803T=	ENSP00000315371.8:p.Cys601=
NM_001142649.1:c.1800T=	NP_001136121.1:p.Cys600=
NM_213599.2:c.1803T= , LRG_868t1:c.1803T=	NP_998764.1:p.Cys601=
XM_005252820.2:c.1761T=	XP_005252877.2:p.Cys587=
XM_005252821.2:c.1758T=	XP_005252878.2:p.Cys586=
XM_005252822.3:c.1725T=	XP_005252879.1:p.Cys575=
XM_005252823.3:c.1722T=	XP_005252880.1:p.Cys574=
XM_011519949.1:c.1710T=	XP_011518251.1:p.Cys570=
XM_005252820.3:c.1761T=	XP_005252877.2:p.Cys587=
XM_005252821.3:c.1758T=	XP_005252878.2:p.Cys586=
XM_005252822.4:c.1725T=	XP_005252879.1:p.Cys575=
XM_011519949.2:c.1710T=	XP_011518251.1:p.Cys570=
NM_001142649.2:c.1800T=	NP_001136121.1:p.Cys600=
NM_213599.3:c.1803T= MANE Select	NP_998764.1:p.Cys601=