Canonical Allele Identifier: CA1957418759

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259650C= , CM000673.2:g.22259650C=	GRCh38
NC_000011.9:g.22281196C= , CM000673.1:g.22281196C=	GRCh37
NC_000011.8:g.22237772C=	NCBI36
NG_015844.1:g.71475C= , LRG_868:g.71475C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1089C=	ENSP00000507766.1:p.Thr363=
ENST00000682341.1:c.1497C=	ENSP00000508251.1:p.Thr499=
ENST00000683197.1:c.1497C=	ENSP00000507641.1:p.Thr499=
ENST00000683411.1:c.1089C=	ENSP00000508397.1:p.Thr363=
ENST00000683437.1:c.1089C=	ENSP00000508408.1:p.Thr363=
ENST00000683613.1:n.2533C=
ENST00000684663.1:c.1494C=	ENSP00000508009.1:p.Thr498=
ENST00000324559.9:c.1539C= MANE Select	ENSP00000315371.9:p.Thr513=
ENST00000648804.1:n.1874C=
ENST00000324559.8:c.1539C=	ENSP00000315371.8:p.Thr513=
NM_001142649.1:c.1536C=	NP_001136121.1:p.Thr512=
NM_213599.2:c.1539C= , LRG_868t1:c.1539C=	NP_998764.1:p.Thr513=
XM_005252820.2:c.1497C=	XP_005252877.2:p.Thr499=
XM_005252821.2:c.1494C=	XP_005252878.2:p.Thr498=
XM_005252822.3:c.1461C=	XP_005252879.1:p.Thr487=
XM_005252823.3:c.1458C=	XP_005252880.1:p.Thr486=
XM_011519949.1:c.1446C=	XP_011518251.1:p.Thr482=
XM_005252820.3:c.1497C=	XP_005252877.2:p.Thr499=
XM_005252821.3:c.1494C=	XP_005252878.2:p.Thr498=
XM_005252822.4:c.1461C=	XP_005252879.1:p.Thr487=
XM_011519949.2:c.1446C=	XP_011518251.1:p.Thr482=
NM_001142649.2:c.1536C=	NP_001136121.1:p.Thr512=
NM_213599.3:c.1539C= MANE Select	NP_998764.1:p.Thr513=