Canonical Allele Identifier: CA473405079

Gene: ANO5

Linked Data

• COSMIC: COSM2112561
• MyVariant Identifiers: chr11:g.22281190G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259644G>A , CM000673.2:g.22259644G>A	GRCh38
NC_000011.9:g.22281190G>A , CM000673.1:g.22281190G>A	GRCh37
NC_000011.8:g.22237766G>A	NCBI36
NG_015844.1:g.71469G>A , LRG_868:g.71469G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1083G>A	ENSP00000507766.1:p.Gln361=
ENST00000682341.1:c.1491G>A	ENSP00000508251.1:p.Gln497=
ENST00000683197.1:c.1491G>A	ENSP00000507641.1:p.Gln497=
ENST00000683411.1:c.1083G>A	ENSP00000508397.1:p.Gln361=
ENST00000683437.1:c.1083G>A	ENSP00000508408.1:p.Gln361=
ENST00000683613.1:n.2527G>A
ENST00000684663.1:c.1488G>A	ENSP00000508009.1:p.Gln496=
ENST00000324559.9:c.1533G>A MANE Select	ENSP00000315371.9:p.Gln511=
ENST00000648804.1:n.1868G>A
ENST00000324559.8:c.1533G>A	ENSP00000315371.8:p.Gln511=
NM_001142649.1:c.1530G>A	NP_001136121.1:p.Gln510=
NM_213599.2:c.1533G>A , LRG_868t1:c.1533G>A	NP_998764.1:p.Gln511=
XM_005252820.2:c.1491G>A	XP_005252877.2:p.Gln497=
XM_005252821.2:c.1488G>A	XP_005252878.2:p.Gln496=
XM_005252822.3:c.1455G>A	XP_005252879.1:p.Gln485=
XM_005252823.3:c.1452G>A	XP_005252880.1:p.Gln484=
XM_011519949.1:c.1440G>A	XP_011518251.1:p.Gln480=
XM_005252820.3:c.1491G>A	XP_005252877.2:p.Gln497=
XM_005252821.3:c.1488G>A	XP_005252878.2:p.Gln496=
XM_005252822.4:c.1455G>A	XP_005252879.1:p.Gln485=
XM_011519949.2:c.1440G>A	XP_011518251.1:p.Gln480=
NM_001142649.2:c.1530G>A	NP_001136121.1:p.Gln510=
NM_213599.3:c.1533G>A MANE Select	NP_998764.1:p.Gln511=