Canonical Allele Identifier: CA3182850073

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22276149C= , CM000673.2:g.22276149C=	GRCh38
NC_000011.9:g.22297695C= , CM000673.1:g.22297695C=	GRCh37
NC_000011.8:g.22254271C=	NCBI36
NG_015844.1:g.87974C= , LRG_868:g.87974C=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.2470C= MANE Select	NP_998764.1:p.Gln824=
ENST00000324559.9:c.2470C= MANE Select	ENSP00000315371.9:p.Gln824=
NM_001142649.1:c.2467C=	NP_001136121.1:p.Gln823=
NM_001142649.2:c.2467C=	NP_001136121.1:p.Gln823=
NM_213599.2:c.2470C= , LRG_868t1:c.2470C=	NP_998764.1:p.Gln824=
ENST00000324559.8:c.2470C=	ENSP00000315371.8:p.Gln824=
ENST00000532043.1:n.487C=
ENST00000532043.2:n.487C=
ENST00000648804.1:n.2805C=
ENST00000682266.1:c.2020C=	ENSP00000507766.1:p.Gln674=
ENST00000682341.1:c.2428C=	ENSP00000508251.1:p.Gln810=
ENST00000683197.1:c.2372+1402C=	ENSP00000507641.1:n.2372+1402C=
ENST00000683411.1:c.2020C=	ENSP00000508397.1:p.Gln674=
ENST00000683437.1:c.2020C=	ENSP00000508408.1:p.Gln674=
ENST00000683613.1:n.3464C=
ENST00000684663.1:c.2425C=	ENSP00000508009.1:p.Gln809=
XM_005252820.2:c.2428C=	XP_005252877.2:p.Gln810=
XM_005252820.3:c.2428C=	XP_005252877.2:p.Gln810=
XM_005252821.2:c.2425C=	XP_005252878.2:p.Gln809=
XM_005252821.3:c.2425C=	XP_005252878.2:p.Gln809=
XM_005252822.3:c.2392C=	XP_005252879.1:p.Gln798=
XM_005252822.4:c.2392C=	XP_005252879.1:p.Gln798=
XM_005252823.3:c.2389C=	XP_005252880.1:p.Gln797=
XM_011519949.1:c.2377C=	XP_011518251.1:p.Gln793=
XM_011519949.2:c.2377C=	XP_011518251.1:p.Gln793=