Canonical Allele Identifier: CA379921431

Gene: ANO5

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.539A>T
ENST00000682266.1:c.769A>T	ENSP00000507766.1:p.Arg257Ter
ENST00000682341.1:c.1177A>T	ENSP00000508251.1:p.Arg393Ter
ENST00000682530.1:c.*1151A>T	ENSP00000506805.1:n.*1151A>T
ENST00000683197.1:c.1177A>T	ENSP00000507641.1:p.Arg393Ter
ENST00000683411.1:c.769A>T	ENSP00000508397.1:p.Arg257Ter
ENST00000683437.1:c.769A>T	ENSP00000508408.1:p.Arg257Ter
ENST00000683613.1:n.2213A>T
ENST00000683834.1:n.1419A>T
ENST00000684663.1:c.1174A>T	ENSP00000508009.1:p.Arg392Ter
ENST00000324559.9:c.1219A>T MANE Select	ENSP00000315371.9:p.Arg407Ter
ENST00000648804.1:n.1554A>T
ENST00000324559.8:c.1219A>T	ENSP00000315371.8:p.Arg407Ter
NM_001142649.1:c.1216A>T	NP_001136121.1:p.Arg406Ter
NM_213599.2:c.1219A>T , LRG_868t1:c.1219A>T	NP_998764.1:p.Arg407Ter
XM_005252820.2:c.1177A>T	XP_005252877.2:p.Arg393Ter
XM_005252821.2:c.1174A>T	XP_005252878.2:p.Arg392Ter
XM_005252822.3:c.1141A>T	XP_005252879.1:p.Arg381Ter
XM_005252823.3:c.1138A>T	XP_005252880.1:p.Arg380Ter
XM_011519949.1:c.1126A>T	XP_011518251.1:p.Arg376Ter
XM_005252820.3:c.1177A>T	XP_005252877.2:p.Arg393Ter
XM_005252821.3:c.1174A>T	XP_005252878.2:p.Arg392Ter
XM_005252822.4:c.1141A>T	XP_005252879.1:p.Arg381Ter
XM_011519949.2:c.1126A>T	XP_011518251.1:p.Arg376Ter
NM_001142649.2:c.1216A>T	NP_001136121.1:p.Arg406Ter
NM_213599.3:c.1219A>T MANE Select	NP_998764.1:p.Arg407Ter