Canonical Allele Identifier: CA1957407616

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22236206G= , CM000673.2:g.22236206G=	GRCh38
NC_000011.9:g.22257752G= , CM000673.1:g.22257752G=	GRCh37
NC_000011.8:g.22214328G=	NCBI36
NG_015844.1:g.48031G= , LRG_868:g.48031G=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.692G= MANE Select	NP_998764.1:p.Gly231=
ENST00000324559.9:c.692G= MANE Select	ENSP00000315371.9:p.Gly231=
NM_001142649.1:c.689G=	NP_001136121.1:p.Gly230=
NM_001142649.2:c.689G=	NP_001136121.1:p.Gly230=
NM_213599.2:c.692G= , LRG_868t1:c.692G=	NP_998764.1:p.Gly231=
ENST00000324559.8:c.692G=	ENSP00000315371.8:p.Gly231=
ENST00000648804.1:n.1213+8620G=
ENST00000682266.1:c.242G=	ENSP00000507766.1:p.Gly81=
ENST00000682341.1:c.650G=	ENSP00000508251.1:p.Gly217=
ENST00000682530.1:c.*624G=	ENSP00000506805.1:n.*624G=
ENST00000682684.1:n.1071G=
ENST00000683197.1:c.650G=	ENSP00000507641.1:p.Gly217=
ENST00000683411.1:c.242G=	ENSP00000508397.1:p.Gly81=
ENST00000683437.1:c.242G=	ENSP00000508408.1:p.Gly81=
ENST00000683613.1:n.1686G=
ENST00000683834.1:n.892G=
ENST00000684663.1:c.647G=	ENSP00000508009.1:p.Gly216=
XM_005252820.2:c.650G=	XP_005252877.2:p.Gly217=
XM_005252820.3:c.650G=	XP_005252877.2:p.Gly217=
XM_005252821.2:c.647G=	XP_005252878.2:p.Gly216=
XM_005252821.3:c.647G=	XP_005252878.2:p.Gly216=
XM_005252822.3:c.614G=	XP_005252879.1:p.Gly205=
XM_005252822.4:c.614G=	XP_005252879.1:p.Gly205=
XM_005252823.3:c.611G=	XP_005252880.1:p.Gly204=
XM_011519949.1:c.599G=	XP_011518251.1:p.Gly200=
XM_011519949.2:c.599G=	XP_011518251.1:p.Gly200=