Canonical Allele Identifier: CA1957403059

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272928A= , CM000673.2:g.22272928A=	GRCh38
NC_000011.9:g.22294474A= , CM000673.1:g.22294474A=	GRCh37
NC_000011.8:g.22251050A=	NCBI36
NG_015844.1:g.84753A= , LRG_868:g.84753A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.191A=
ENST00000682266.1:c.1724A=	ENSP00000507766.1:p.His575=
ENST00000682341.1:c.2132A=	ENSP00000508251.1:p.His711=
ENST00000683197.1:c.2132A=	ENSP00000507641.1:p.His711=
ENST00000683411.1:c.1724A=	ENSP00000508397.1:p.His575=
ENST00000683437.1:c.1724A=	ENSP00000508408.1:p.His575=
ENST00000683613.1:n.3168A=
ENST00000684663.1:c.2129A=	ENSP00000508009.1:p.His710=
ENST00000324559.9:c.2174A= MANE Select	ENSP00000315371.9:p.His725=
ENST00000648804.1:n.2509A=
ENST00000324559.8:c.2174A=	ENSP00000315371.8:p.His725=
ENST00000532043.1:n.191A=
NM_001142649.1:c.2171A=	NP_001136121.1:p.His724=
NM_213599.2:c.2174A= , LRG_868t1:c.2174A=	NP_998764.1:p.His725=
XM_005252820.2:c.2132A=	XP_005252877.2:p.His711=
XM_005252821.2:c.2129A=	XP_005252878.2:p.His710=
XM_005252822.3:c.2096A=	XP_005252879.1:p.His699=
XM_005252823.3:c.2093A=	XP_005252880.1:p.His698=
XM_011519949.1:c.2081A=	XP_011518251.1:p.His694=
XM_005252820.3:c.2132A=	XP_005252877.2:p.His711=
XM_005252821.3:c.2129A=	XP_005252878.2:p.His710=
XM_005252822.4:c.2096A=	XP_005252879.1:p.His699=
XM_011519949.2:c.2081A=	XP_011518251.1:p.His694=
NM_001142649.2:c.2171A=	NP_001136121.1:p.His724=
NM_213599.3:c.2174A= MANE Select	NP_998764.1:p.His725=