Canonical Allele Identifier: CA1957416921

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255410G= , CM000673.2:g.22255410G=	GRCh38
NC_000011.9:g.22276956G= , CM000673.1:g.22276956G=	GRCh37
NC_000011.8:g.22233532G=	NCBI36
NG_015844.1:g.67235G= , LRG_868:g.67235G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.540G=
ENST00000682266.1:c.770G=	ENSP00000507766.1:p.Arg257=
ENST00000682341.1:c.1178G=	ENSP00000508251.1:p.Arg393=
ENST00000682530.1:c.*1152G=	ENSP00000506805.1:n.*1152G=
ENST00000683197.1:c.1178G=	ENSP00000507641.1:p.Arg393=
ENST00000683411.1:c.770G=	ENSP00000508397.1:p.Arg257=
ENST00000683437.1:c.770G=	ENSP00000508408.1:p.Arg257=
ENST00000683613.1:n.2214G=
ENST00000683834.1:n.1420G=
ENST00000684663.1:c.1175G=	ENSP00000508009.1:p.Arg392=
ENST00000324559.9:c.1220G= MANE Select	ENSP00000315371.9:p.Arg407=
ENST00000648804.1:n.1555G=
ENST00000324559.8:c.1220G=	ENSP00000315371.8:p.Arg407=
NM_001142649.1:c.1217G=	NP_001136121.1:p.Arg406=
NM_213599.2:c.1220G= , LRG_868t1:c.1220G=	NP_998764.1:p.Arg407=
XM_005252820.2:c.1178G=	XP_005252877.2:p.Arg393=
XM_005252821.2:c.1175G=	XP_005252878.2:p.Arg392=
XM_005252822.3:c.1142G=	XP_005252879.1:p.Arg381=
XM_005252823.3:c.1139G=	XP_005252880.1:p.Arg380=
XM_011519949.1:c.1127G=	XP_011518251.1:p.Arg376=
XM_005252820.3:c.1178G=	XP_005252877.2:p.Arg393=
XM_005252821.3:c.1175G=	XP_005252878.2:p.Arg392=
XM_005252822.4:c.1142G=	XP_005252879.1:p.Arg381=
XM_011519949.2:c.1127G=	XP_011518251.1:p.Arg376=
NM_001142649.2:c.1217G=	NP_001136121.1:p.Arg406=
NM_213599.3:c.1220G= MANE Select	NP_998764.1:p.Arg407=