Canonical Allele Identifier: CA1957402803

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272839T= , CM000673.2:g.22272839T=	GRCh38
NC_000011.9:g.22294385T= , CM000673.1:g.22294385T=	GRCh37
NC_000011.8:g.22250961T=	NCBI36
NG_015844.1:g.84664T= , LRG_868:g.84664T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.102T=
ENST00000682266.1:c.1635T=	ENSP00000507766.1:p.Leu545=
ENST00000682341.1:c.2043T=	ENSP00000508251.1:p.Leu681=
ENST00000683197.1:c.2043T=	ENSP00000507641.1:p.Leu681=
ENST00000683411.1:c.1635T=	ENSP00000508397.1:p.Leu545=
ENST00000683437.1:c.1635T=	ENSP00000508408.1:p.Leu545=
ENST00000683613.1:n.3079T=
ENST00000684663.1:c.2040T=	ENSP00000508009.1:p.Leu680=
ENST00000324559.9:c.2085T= MANE Select	ENSP00000315371.9:p.Leu695=
ENST00000648804.1:n.2420T=
ENST00000324559.8:c.2085T=	ENSP00000315371.8:p.Leu695=
ENST00000532043.1:n.102T=
NM_001142649.1:c.2082T=	NP_001136121.1:p.Leu694=
NM_213599.2:c.2085T= , LRG_868t1:c.2085T=	NP_998764.1:p.Leu695=
XM_005252820.2:c.2043T=	XP_005252877.2:p.Leu681=
XM_005252821.2:c.2040T=	XP_005252878.2:p.Leu680=
XM_005252822.3:c.2007T=	XP_005252879.1:p.Leu669=
XM_005252823.3:c.2004T=	XP_005252880.1:p.Leu668=
XM_011519949.1:c.1992T=	XP_011518251.1:p.Leu664=
XM_005252820.3:c.2043T=	XP_005252877.2:p.Leu681=
XM_005252821.3:c.2040T=	XP_005252878.2:p.Leu680=
XM_005252822.4:c.2007T=	XP_005252879.1:p.Leu669=
XM_011519949.2:c.1992T=	XP_011518251.1:p.Leu664=
NM_001142649.2:c.2082T=	NP_001136121.1:p.Leu694=
NM_213599.3:c.2085T= MANE Select	NP_998764.1:p.Leu695=