Canonical Allele Identifier: CA5922986

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22236170A>G , CM000673.2:g.22236170A>G	GRCh38
NC_000011.9:g.22257716A>G , CM000673.1:g.22257716A>G	GRCh37
NC_000011.8:g.22214292A>G	NCBI36
NG_015844.1:g.47995A>G , LRG_868:g.47995A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.656A>G MANE Select	NP_998764.1:p.Tyr219Cys
ENST00000324559.9:c.656A>G MANE Select	ENSP00000315371.9:p.Tyr219Cys
NM_001142649.1:c.653A>G	NP_001136121.1:p.Tyr218Cys
NM_001142649.2:c.653A>G	NP_001136121.1:p.Tyr218Cys
NM_213599.2:c.656A>G , LRG_868t1:c.656A>G	NP_998764.1:p.Tyr219Cys
ENST00000324559.8:c.656A>G	ENSP00000315371.8:p.Tyr219Cys
ENST00000648804.1:n.1213+8584A>G
ENST00000682266.1:c.206A>G	ENSP00000507766.1:p.Tyr69Cys
ENST00000682341.1:c.614A>G	ENSP00000508251.1:p.Tyr205Cys
ENST00000682530.1:c.*588A>G	ENSP00000506805.1:n.*588A>G
ENST00000682684.1:n.1035A>G
ENST00000683197.1:c.614A>G	ENSP00000507641.1:p.Tyr205Cys
ENST00000683411.1:c.206A>G	ENSP00000508397.1:p.Tyr69Cys
ENST00000683437.1:c.206A>G	ENSP00000508408.1:p.Tyr69Cys
ENST00000683613.1:n.1650A>G
ENST00000683834.1:n.856A>G
ENST00000684663.1:c.611A>G	ENSP00000508009.1:p.Tyr204Cys
XM_005252820.2:c.614A>G	XP_005252877.2:p.Tyr205Cys
XM_005252820.3:c.614A>G	XP_005252877.2:p.Tyr205Cys
XM_005252821.2:c.611A>G	XP_005252878.2:p.Tyr204Cys
XM_005252821.3:c.611A>G	XP_005252878.2:p.Tyr204Cys
XM_005252822.3:c.578A>G	XP_005252879.1:p.Tyr193Cys
XM_005252822.4:c.578A>G	XP_005252879.1:p.Tyr193Cys
XM_005252823.3:c.575A>G	XP_005252880.1:p.Tyr192Cys
XM_011519949.1:c.563A>G	XP_011518251.1:p.Tyr188Cys
XM_011519949.2:c.563A>G	XP_011518251.1:p.Tyr188Cys