Canonical Allele Identifier: CA379920926

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22271915C>G (hg19) ; chr11:g.22250369C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250369C>G , CM000673.2:g.22250369C>G	GRCh38
NC_000011.9:g.22271915C>G , CM000673.1:g.22271915C>G	GRCh37
NC_000011.8:g.22228491C>G	NCBI36
NG_015844.1:g.62194C>G , LRG_868:g.62194C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.331C>G
ENST00000682266.1:c.561C>G	ENSP00000507766.1:p.Ser187Arg
ENST00000682341.1:c.969C>G	ENSP00000508251.1:p.Ser323Arg
ENST00000682530.1:c.*943C>G	ENSP00000506805.1:n.*943C>G
ENST00000683197.1:c.969C>G	ENSP00000507641.1:p.Ser323Arg
ENST00000683411.1:c.561C>G	ENSP00000508397.1:p.Ser187Arg
ENST00000683437.1:c.561C>G	ENSP00000508408.1:p.Ser187Arg
ENST00000683613.1:n.2005C>G
ENST00000683834.1:n.1211C>G
ENST00000684663.1:c.966C>G	ENSP00000508009.1:p.Ser322Arg
ENST00000324559.9:c.1011C>G MANE Select	ENSP00000315371.9:p.Ser337Arg
ENST00000648804.1:n.1346C>G
ENST00000324559.8:c.1011C>G	ENSP00000315371.8:p.Ser337Arg
NM_001142649.1:c.1008C>G	NP_001136121.1:p.Ser336Arg
NM_213599.2:c.1011C>G , LRG_868t1:c.1011C>G	NP_998764.1:p.Ser337Arg
XM_005252820.2:c.969C>G	XP_005252877.2:p.Ser323Arg
XM_005252821.2:c.966C>G	XP_005252878.2:p.Ser322Arg
XM_005252822.3:c.933C>G	XP_005252879.1:p.Ser311Arg
XM_005252823.3:c.930C>G	XP_005252880.1:p.Ser310Arg
XM_011519949.1:c.918C>G	XP_011518251.1:p.Ser306Arg
XM_005252820.3:c.969C>G	XP_005252877.2:p.Ser323Arg
XM_005252821.3:c.966C>G	XP_005252878.2:p.Ser322Arg
XM_005252822.4:c.933C>G	XP_005252879.1:p.Ser311Arg
XM_011519949.2:c.918C>G	XP_011518251.1:p.Ser306Arg
NM_001142649.2:c.1008C>G	NP_001136121.1:p.Ser336Arg
NM_213599.3:c.1011C>G MANE Select	NP_998764.1:p.Ser337Arg