Canonical Allele Identifier: CA1957418771

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259673T= , CM000673.2:g.22259673T=	GRCh38
NC_000011.9:g.22281219T= , CM000673.1:g.22281219T=	GRCh37
NC_000011.8:g.22237795T=	NCBI36
NG_015844.1:g.71498T= , LRG_868:g.71498T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1112T=	ENSP00000507766.1:p.Leu371=
ENST00000682341.1:c.1520T=	ENSP00000508251.1:p.Leu507=
ENST00000683197.1:c.1520T=	ENSP00000507641.1:p.Leu507=
ENST00000683411.1:c.1112T=	ENSP00000508397.1:p.Leu371=
ENST00000683437.1:c.1112T=	ENSP00000508408.1:p.Leu371=
ENST00000683613.1:n.2556T=
ENST00000684663.1:c.1517T=	ENSP00000508009.1:p.Leu506=
ENST00000324559.9:c.1562T= MANE Select	ENSP00000315371.9:p.Leu521=
ENST00000648804.1:n.1897T=
ENST00000324559.8:c.1562T=	ENSP00000315371.8:p.Leu521=
NM_001142649.1:c.1559T=	NP_001136121.1:p.Leu520=
NM_213599.2:c.1562T= , LRG_868t1:c.1562T=	NP_998764.1:p.Leu521=
XM_005252820.2:c.1520T=	XP_005252877.2:p.Leu507=
XM_005252821.2:c.1517T=	XP_005252878.2:p.Leu506=
XM_005252822.3:c.1484T=	XP_005252879.1:p.Leu495=
XM_005252823.3:c.1481T=	XP_005252880.1:p.Leu494=
XM_011519949.1:c.1469T=	XP_011518251.1:p.Leu490=
XM_005252820.3:c.1520T=	XP_005252877.2:p.Leu507=
XM_005252821.3:c.1517T=	XP_005252878.2:p.Leu506=
XM_005252822.4:c.1484T=	XP_005252879.1:p.Leu495=
XM_011519949.2:c.1469T=	XP_011518251.1:p.Leu490=
NM_001142649.2:c.1559T=	NP_001136121.1:p.Leu520=
NM_213599.3:c.1562T= MANE Select	NP_998764.1:p.Leu521=