Canonical Allele Identifier: CA1957420230

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22263056T= , CM000673.2:g.22263056T=	GRCh38
NC_000011.9:g.22284602T= , CM000673.1:g.22284602T=	GRCh37
NC_000011.8:g.22241178T=	NCBI36
NG_015844.1:g.74881T= , LRG_868:g.74881T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1448+13T=	ENSP00000507766.1:n.1448+13T=
ENST00000682341.1:c.1856+13T=	ENSP00000508251.1:n.1856+13T=
ENST00000683197.1:c.1856+13T=	ENSP00000507641.1:n.1856+13T=
ENST00000683411.1:c.1448+13T=	ENSP00000508397.1:n.1448+13T=
ENST00000683437.1:c.1448+13T=	ENSP00000508408.1:n.1448+13T=
ENST00000683613.1:n.2892+13T=
ENST00000684663.1:c.1853+13T=	ENSP00000508009.1:n.1853+13T=
ENST00000324559.9:c.1898+13T= MANE Select	ENSP00000315371.9:n.1898+13T=
ENST00000648804.1:n.2233+13T=
ENST00000324559.8:c.1898+13T=	ENSP00000315371.8:n.1898+13T=
NM_001142649.1:c.1895+13T=	NP_001136121.1:n.1895+13T=
NM_213599.2:c.1898+13T= , LRG_868t1:c.1898+13T=	NP_998764.1:n.1898+13T=
XM_005252820.2:c.1856+13T=	XP_005252877.2:n.1856+13T=
XM_005252821.2:c.1853+13T=	XP_005252878.2:n.1853+13T=
XM_005252822.3:c.1820+13T=	XP_005252879.1:n.1820+13T=
XM_005252823.3:c.1817+13T=	XP_005252880.1:n.1817+13T=
XM_011519949.1:c.1805+13T=	XP_011518251.1:n.1805+13T=
XM_005252820.3:c.1856+13T=	XP_005252877.2:n.1856+13T=
XM_005252821.3:c.1853+13T=	XP_005252878.2:n.1853+13T=
XM_005252822.4:c.1820+13T=	XP_005252879.1:n.1820+13T=
XM_011519949.2:c.1805+13T=	XP_011518251.1:n.1805+13T=
NM_001142649.2:c.1895+13T=	NP_001136121.1:n.1895+13T=
NM_213599.3:c.1898+13T= MANE Select	NP_998764.1:n.1898+13T=