Canonical Allele Identifier: CA473404025

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22271798A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250252A>G , CM000673.2:g.22250252A>G	GRCh38
NC_000011.9:g.22271798A>G , CM000673.1:g.22271798A>G	GRCh37
NC_000011.8:g.22228374A>G	NCBI36
NG_015844.1:g.62077A>G , LRG_868:g.62077A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.214A>G
ENST00000682266.1:c.444A>G	ENSP00000507766.1:p.Glu148=
ENST00000682341.1:c.852A>G	ENSP00000508251.1:p.Glu284=
ENST00000682530.1:c.*826A>G	ENSP00000506805.1:n.*826A>G
ENST00000683197.1:c.852A>G	ENSP00000507641.1:p.Glu284=
ENST00000683411.1:c.444A>G	ENSP00000508397.1:p.Glu148=
ENST00000683437.1:c.444A>G	ENSP00000508408.1:p.Glu148=
ENST00000683613.1:n.1888A>G
ENST00000683834.1:n.1094A>G
ENST00000684663.1:c.849A>G	ENSP00000508009.1:p.Glu283=
ENST00000324559.9:c.894A>G MANE Select	ENSP00000315371.9:p.Glu298=
ENST00000648804.1:n.1229A>G
ENST00000324559.8:c.894A>G	ENSP00000315371.8:p.Glu298=
NM_001142649.1:c.891A>G	NP_001136121.1:p.Glu297=
NM_213599.2:c.894A>G , LRG_868t1:c.894A>G	NP_998764.1:p.Glu298=
XM_005252820.2:c.852A>G	XP_005252877.2:p.Glu284=
XM_005252821.2:c.849A>G	XP_005252878.2:p.Glu283=
XM_005252822.3:c.816A>G	XP_005252879.1:p.Glu272=
XM_005252823.3:c.813A>G	XP_005252880.1:p.Glu271=
XM_011519949.1:c.801A>G	XP_011518251.1:p.Glu267=
XM_005252820.3:c.852A>G	XP_005252877.2:p.Glu284=
XM_005252821.3:c.849A>G	XP_005252878.2:p.Glu283=
XM_005252822.4:c.816A>G	XP_005252879.1:p.Glu272=
XM_011519949.2:c.801A>G	XP_011518251.1:p.Glu267=
NM_001142649.2:c.891A>G	NP_001136121.1:p.Glu297=
NM_213599.3:c.894A>G MANE Select	NP_998764.1:p.Glu298=