Canonical Allele Identifier: CA1957416916

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255400C= , CM000673.2:g.22255400C=	GRCh38
NC_000011.9:g.22276946C= , CM000673.1:g.22276946C=	GRCh37
NC_000011.8:g.22233522C=	NCBI36
NG_015844.1:g.67225C= , LRG_868:g.67225C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.530C=
ENST00000682266.1:c.760C=	ENSP00000507766.1:p.Arg254=
ENST00000682341.1:c.1168C=	ENSP00000508251.1:p.Arg390=
ENST00000682530.1:c.*1142C=	ENSP00000506805.1:n.*1142C=
ENST00000683197.1:c.1168C=	ENSP00000507641.1:p.Arg390=
ENST00000683411.1:c.760C=	ENSP00000508397.1:p.Arg254=
ENST00000683437.1:c.760C=	ENSP00000508408.1:p.Arg254=
ENST00000683613.1:n.2204C=
ENST00000683834.1:n.1410C=
ENST00000684663.1:c.1165C=	ENSP00000508009.1:p.Arg389=
ENST00000324559.9:c.1210C= MANE Select	ENSP00000315371.9:p.Arg404=
ENST00000648804.1:n.1545C=
ENST00000324559.8:c.1210C=	ENSP00000315371.8:p.Arg404=
NM_001142649.1:c.1207C=	NP_001136121.1:p.Arg403=
NM_213599.2:c.1210C= , LRG_868t1:c.1210C=	NP_998764.1:p.Arg404=
XM_005252820.2:c.1168C=	XP_005252877.2:p.Arg390=
XM_005252821.2:c.1165C=	XP_005252878.2:p.Arg389=
XM_005252822.3:c.1132C=	XP_005252879.1:p.Arg378=
XM_005252823.3:c.1129C=	XP_005252880.1:p.Arg377=
XM_011519949.1:c.1117C=	XP_011518251.1:p.Arg373=
XM_005252820.3:c.1168C=	XP_005252877.2:p.Arg390=
XM_005252821.3:c.1165C=	XP_005252878.2:p.Arg389=
XM_005252822.4:c.1132C=	XP_005252879.1:p.Arg378=
XM_011519949.2:c.1117C=	XP_011518251.1:p.Arg373=
NM_001142649.2:c.1207C=	NP_001136121.1:p.Arg403=
NM_213599.3:c.1210C= MANE Select	NP_998764.1:p.Arg404=