Canonical Allele Identifier: CA379921430

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22276955A>G (hg19) ; chr11:g.22255409A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255409A>G , CM000673.2:g.22255409A>G	GRCh38
NC_000011.9:g.22276955A>G , CM000673.1:g.22276955A>G	GRCh37
NC_000011.8:g.22233531A>G	NCBI36
NG_015844.1:g.67234A>G , LRG_868:g.67234A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.539A>G
ENST00000682266.1:c.769A>G	ENSP00000507766.1:p.Arg257Gly
ENST00000682341.1:c.1177A>G	ENSP00000508251.1:p.Arg393Gly
ENST00000682530.1:c.*1151A>G	ENSP00000506805.1:n.*1151A>G
ENST00000683197.1:c.1177A>G	ENSP00000507641.1:p.Arg393Gly
ENST00000683411.1:c.769A>G	ENSP00000508397.1:p.Arg257Gly
ENST00000683437.1:c.769A>G	ENSP00000508408.1:p.Arg257Gly
ENST00000683613.1:n.2213A>G
ENST00000683834.1:n.1419A>G
ENST00000684663.1:c.1174A>G	ENSP00000508009.1:p.Arg392Gly
ENST00000324559.9:c.1219A>G MANE Select	ENSP00000315371.9:p.Arg407Gly
ENST00000648804.1:n.1554A>G
ENST00000324559.8:c.1219A>G	ENSP00000315371.8:p.Arg407Gly
NM_001142649.1:c.1216A>G	NP_001136121.1:p.Arg406Gly
NM_213599.2:c.1219A>G , LRG_868t1:c.1219A>G	NP_998764.1:p.Arg407Gly
XM_005252820.2:c.1177A>G	XP_005252877.2:p.Arg393Gly
XM_005252821.2:c.1174A>G	XP_005252878.2:p.Arg392Gly
XM_005252822.3:c.1141A>G	XP_005252879.1:p.Arg381Gly
XM_005252823.3:c.1138A>G	XP_005252880.1:p.Arg380Gly
XM_011519949.1:c.1126A>G	XP_011518251.1:p.Arg376Gly
XM_005252820.3:c.1177A>G	XP_005252877.2:p.Arg393Gly
XM_005252821.3:c.1174A>G	XP_005252878.2:p.Arg392Gly
XM_005252822.4:c.1141A>G	XP_005252879.1:p.Arg381Gly
XM_011519949.2:c.1126A>G	XP_011518251.1:p.Arg376Gly
NM_001142649.2:c.1216A>G	NP_001136121.1:p.Arg406Gly
NM_213599.3:c.1219A>G MANE Select	NP_998764.1:p.Arg407Gly