Canonical Allele Identifier: CA473404013

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22271795A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250249A>T , CM000673.2:g.22250249A>T	GRCh38
NC_000011.9:g.22271795A>T , CM000673.1:g.22271795A>T	GRCh37
NC_000011.8:g.22228371A>T	NCBI36
NG_015844.1:g.62074A>T , LRG_868:g.62074A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.211A>T
ENST00000682266.1:c.441A>T	ENSP00000507766.1:p.Gly147=
ENST00000682341.1:c.849A>T	ENSP00000508251.1:p.Gly283=
ENST00000682530.1:c.*823A>T	ENSP00000506805.1:n.*823A>T
ENST00000683197.1:c.849A>T	ENSP00000507641.1:p.Gly283=
ENST00000683411.1:c.441A>T	ENSP00000508397.1:p.Gly147=
ENST00000683437.1:c.441A>T	ENSP00000508408.1:p.Gly147=
ENST00000683613.1:n.1885A>T
ENST00000683834.1:n.1091A>T
ENST00000684663.1:c.846A>T	ENSP00000508009.1:p.Gly282=
ENST00000324559.9:c.891A>T MANE Select	ENSP00000315371.9:p.Gly297=
ENST00000648804.1:n.1226A>T
ENST00000324559.8:c.891A>T	ENSP00000315371.8:p.Gly297=
NM_001142649.1:c.888A>T	NP_001136121.1:p.Gly296=
NM_213599.2:c.891A>T , LRG_868t1:c.891A>T	NP_998764.1:p.Gly297=
XM_005252820.2:c.849A>T	XP_005252877.2:p.Gly283=
XM_005252821.2:c.846A>T	XP_005252878.2:p.Gly282=
XM_005252822.3:c.813A>T	XP_005252879.1:p.Gly271=
XM_005252823.3:c.810A>T	XP_005252880.1:p.Gly270=
XM_011519949.1:c.798A>T	XP_011518251.1:p.Gly266=
XM_005252820.3:c.849A>T	XP_005252877.2:p.Gly283=
XM_005252821.3:c.846A>T	XP_005252878.2:p.Gly282=
XM_005252822.4:c.813A>T	XP_005252879.1:p.Gly271=
XM_011519949.2:c.798A>T	XP_011518251.1:p.Gly266=
NM_001142649.2:c.888A>T	NP_001136121.1:p.Gly296=
NM_213599.3:c.891A>T MANE Select	NP_998764.1:p.Gly297=