Canonical Allele Identifier: CA1957417920

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22257738C= , CM000673.2:g.22257738C=	GRCh38
NC_000011.9:g.22279284C= , CM000673.1:g.22279284C=	GRCh37
NC_000011.8:g.22235860C=	NCBI36
NG_015844.1:g.69563C= , LRG_868:g.69563C=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1391C= MANE Select	NP_998764.1:p.Ala464=
ENST00000324559.9:c.1391C= MANE Select	ENSP00000315371.9:p.Ala464=
NM_001142649.1:c.1388C=	NP_001136121.1:p.Ala463=
NM_001142649.2:c.1388C=	NP_001136121.1:p.Ala463=
NM_213599.2:c.1391C= , LRG_868t1:c.1391C=	NP_998764.1:p.Ala464=
ENST00000324559.8:c.1391C=	ENSP00000315371.8:p.Ala464=
ENST00000648804.1:n.1726C=
ENST00000682266.1:c.941C=	ENSP00000507766.1:p.Ala314=
ENST00000682341.1:c.1349C=	ENSP00000508251.1:p.Ala450=
ENST00000683197.1:c.1349C=	ENSP00000507641.1:p.Ala450=
ENST00000683411.1:c.941C=	ENSP00000508397.1:p.Ala314=
ENST00000683437.1:c.941C=	ENSP00000508408.1:p.Ala314=
ENST00000683613.1:n.2385C=
ENST00000684663.1:c.1346C=	ENSP00000508009.1:p.Ala449=
XM_005252820.2:c.1349C=	XP_005252877.2:p.Ala450=
XM_005252820.3:c.1349C=	XP_005252877.2:p.Ala450=
XM_005252821.2:c.1346C=	XP_005252878.2:p.Ala449=
XM_005252821.3:c.1346C=	XP_005252878.2:p.Ala449=
XM_005252822.3:c.1313C=	XP_005252879.1:p.Ala438=
XM_005252822.4:c.1313C=	XP_005252879.1:p.Ala438=
XM_005252823.3:c.1310C=	XP_005252880.1:p.Ala437=
XM_011519949.1:c.1298C=	XP_011518251.1:p.Ala433=
XM_011519949.2:c.1298C=	XP_011518251.1:p.Ala433=