Canonical Allele Identifier: CA379920161

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22257732T>A (hg19) ; chr11:g.22236186T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22236186T>A , CM000673.2:g.22236186T>A	GRCh38
NC_000011.9:g.22257732T>A , CM000673.1:g.22257732T>A	GRCh37
NC_000011.8:g.22214308T>A	NCBI36
NG_015844.1:g.48011T>A , LRG_868:g.48011T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.222T>A	ENSP00000507766.1:p.Cys74Ter
ENST00000682341.1:c.630T>A	ENSP00000508251.1:p.Cys210Ter
ENST00000682530.1:c.*604T>A	ENSP00000506805.1:n.*604T>A
ENST00000682684.1:n.1051T>A
ENST00000683197.1:c.630T>A	ENSP00000507641.1:p.Cys210Ter
ENST00000683411.1:c.222T>A	ENSP00000508397.1:p.Cys74Ter
ENST00000683437.1:c.222T>A	ENSP00000508408.1:p.Cys74Ter
ENST00000683613.1:n.1666T>A
ENST00000683834.1:n.872T>A
ENST00000684663.1:c.627T>A	ENSP00000508009.1:p.Cys209Ter
ENST00000324559.9:c.672T>A MANE Select	ENSP00000315371.9:p.Cys224Ter
ENST00000648804.1:n.1213+8600T>A
ENST00000324559.8:c.672T>A	ENSP00000315371.8:p.Cys224Ter
NM_001142649.1:c.669T>A	NP_001136121.1:p.Cys223Ter
NM_213599.2:c.672T>A , LRG_868t1:c.672T>A	NP_998764.1:p.Cys224Ter
XM_005252820.2:c.630T>A	XP_005252877.2:p.Cys210Ter
XM_005252821.2:c.627T>A	XP_005252878.2:p.Cys209Ter
XM_005252822.3:c.594T>A	XP_005252879.1:p.Cys198Ter
XM_005252823.3:c.591T>A	XP_005252880.1:p.Cys197Ter
XM_011519949.1:c.579T>A	XP_011518251.1:p.Cys193Ter
XM_005252820.3:c.630T>A	XP_005252877.2:p.Cys210Ter
XM_005252821.3:c.627T>A	XP_005252878.2:p.Cys209Ter
XM_005252822.4:c.594T>A	XP_005252879.1:p.Cys198Ter
XM_011519949.2:c.579T>A	XP_011518251.1:p.Cys193Ter
NM_001142649.2:c.669T>A	NP_001136121.1:p.Cys223Ter
NM_213599.3:c.672T>A MANE Select	NP_998764.1:p.Cys224Ter