Canonical Allele Identifier: CA1957418757

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259647A= , CM000673.2:g.22259647A=	GRCh38
NC_000011.9:g.22281193A= , CM000673.1:g.22281193A=	GRCh37
NC_000011.8:g.22237769A=	NCBI36
NG_015844.1:g.71472A= , LRG_868:g.71472A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1086A=	ENSP00000507766.1:p.Ile362=
ENST00000682341.1:c.1494A=	ENSP00000508251.1:p.Ile498=
ENST00000683197.1:c.1494A=	ENSP00000507641.1:p.Ile498=
ENST00000683411.1:c.1086A=	ENSP00000508397.1:p.Ile362=
ENST00000683437.1:c.1086A=	ENSP00000508408.1:p.Ile362=
ENST00000683613.1:n.2530A=
ENST00000684663.1:c.1491A=	ENSP00000508009.1:p.Ile497=
ENST00000324559.9:c.1536A= MANE Select	ENSP00000315371.9:p.Ile512=
ENST00000648804.1:n.1871A=
ENST00000324559.8:c.1536A=	ENSP00000315371.8:p.Ile512=
NM_001142649.1:c.1533A=	NP_001136121.1:p.Ile511=
NM_213599.2:c.1536A= , LRG_868t1:c.1536A=	NP_998764.1:p.Ile512=
XM_005252820.2:c.1494A=	XP_005252877.2:p.Ile498=
XM_005252821.2:c.1491A=	XP_005252878.2:p.Ile497=
XM_005252822.3:c.1458A=	XP_005252879.1:p.Ile486=
XM_005252823.3:c.1455A=	XP_005252880.1:p.Ile485=
XM_011519949.1:c.1443A=	XP_011518251.1:p.Ile481=
XM_005252820.3:c.1494A=	XP_005252877.2:p.Ile498=
XM_005252821.3:c.1491A=	XP_005252878.2:p.Ile497=
XM_005252822.4:c.1458A=	XP_005252879.1:p.Ile486=
XM_011519949.2:c.1443A=	XP_011518251.1:p.Ile481=
NM_001142649.2:c.1533A=	NP_001136121.1:p.Ile511=
NM_213599.3:c.1536A= MANE Select	NP_998764.1:p.Ile512=