Canonical Allele Identifier: CA1957413158

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250246T= , CM000673.2:g.22250246T=	GRCh38
NC_000011.9:g.22271792T= , CM000673.1:g.22271792T=	GRCh37
NC_000011.8:g.22228368T=	NCBI36
NG_015844.1:g.62071T= , LRG_868:g.62071T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.208T=
ENST00000682266.1:c.438T=	ENSP00000507766.1:p.Tyr146=
ENST00000682341.1:c.846T=	ENSP00000508251.1:p.Tyr282=
ENST00000682530.1:c.*820T=	ENSP00000506805.1:n.*820T=
ENST00000683197.1:c.846T=	ENSP00000507641.1:p.Tyr282=
ENST00000683411.1:c.438T=	ENSP00000508397.1:p.Tyr146=
ENST00000683437.1:c.438T=	ENSP00000508408.1:p.Tyr146=
ENST00000683613.1:n.1882T=
ENST00000683834.1:n.1088T=
ENST00000684663.1:c.843T=	ENSP00000508009.1:p.Tyr281=
ENST00000324559.9:c.888T= MANE Select	ENSP00000315371.9:p.Tyr296=
ENST00000648804.1:n.1223T=
ENST00000324559.8:c.888T=	ENSP00000315371.8:p.Tyr296=
NM_001142649.1:c.885T=	NP_001136121.1:p.Tyr295=
NM_213599.2:c.888T= , LRG_868t1:c.888T=	NP_998764.1:p.Tyr296=
XM_005252820.2:c.846T=	XP_005252877.2:p.Tyr282=
XM_005252821.2:c.843T=	XP_005252878.2:p.Tyr281=
XM_005252822.3:c.810T=	XP_005252879.1:p.Tyr270=
XM_005252823.3:c.807T=	XP_005252880.1:p.Tyr269=
XM_011519949.1:c.795T=	XP_011518251.1:p.Tyr265=
XM_005252820.3:c.846T=	XP_005252877.2:p.Tyr282=
XM_005252821.3:c.843T=	XP_005252878.2:p.Tyr281=
XM_005252822.4:c.810T=	XP_005252879.1:p.Tyr270=
XM_011519949.2:c.795T=	XP_011518251.1:p.Tyr265=
NM_001142649.2:c.885T=	NP_001136121.1:p.Tyr295=
NM_213599.3:c.888T= MANE Select	NP_998764.1:p.Tyr296=