Canonical Allele Identifier: CA1957418726

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259560C= , CM000673.2:g.22259560C=	GRCh38
NC_000011.9:g.22281106C= , CM000673.1:g.22281106C=	GRCh37
NC_000011.8:g.22237682C=	NCBI36
NG_015844.1:g.71385C= , LRG_868:g.71385C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.999C=	ENSP00000507766.1:p.Tyr333=
ENST00000682341.1:c.1407C=	ENSP00000508251.1:p.Tyr469=
ENST00000683197.1:c.1407C=	ENSP00000507641.1:p.Tyr469=
ENST00000683411.1:c.999C=	ENSP00000508397.1:p.Tyr333=
ENST00000683437.1:c.999C=	ENSP00000508408.1:p.Tyr333=
ENST00000683613.1:n.2443C=
ENST00000684663.1:c.1404C=	ENSP00000508009.1:p.Tyr468=
ENST00000324559.9:c.1449C= MANE Select	ENSP00000315371.9:p.Tyr483=
ENST00000648804.1:n.1784C=
ENST00000324559.8:c.1449C=	ENSP00000315371.8:p.Tyr483=
NM_001142649.1:c.1446C=	NP_001136121.1:p.Tyr482=
NM_213599.2:c.1449C= , LRG_868t1:c.1449C=	NP_998764.1:p.Tyr483=
XM_005252820.2:c.1407C=	XP_005252877.2:p.Tyr469=
XM_005252821.2:c.1404C=	XP_005252878.2:p.Tyr468=
XM_005252822.3:c.1371C=	XP_005252879.1:p.Tyr457=
XM_005252823.3:c.1368C=	XP_005252880.1:p.Tyr456=
XM_011519949.1:c.1356C=	XP_011518251.1:p.Tyr452=
XM_005252820.3:c.1407C=	XP_005252877.2:p.Tyr469=
XM_005252821.3:c.1404C=	XP_005252878.2:p.Tyr468=
XM_005252822.4:c.1371C=	XP_005252879.1:p.Tyr457=
XM_011519949.2:c.1356C=	XP_011518251.1:p.Tyr452=
NM_001142649.2:c.1446C=	NP_001136121.1:p.Tyr482=
NM_213599.3:c.1449C= MANE Select	NP_998764.1:p.Tyr483=