Canonical Allele Identifier: CA2535747667
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22218044_22218045insAATAGTGA , CM000673.2:g.22218044_22218045insAATAGTGA GRCh38
NC_000011.9:g.22239590_22239591insAATAGTGA , CM000673.1:g.22239590_22239591insAATAGTGA GRCh37
NC_000011.8:g.22196166_22196167insAATAGTGA NCBI36
NG_015844.1:g.29869_29870insAATAGTGA , LRG_868:g.29869_29870insAATAGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000682084.1:n.3313-202_3313-201insAATAGTGA
ENST00000682266.1:c.-270-3053_-270-3052insAATAGTGA ENSP00000507766.1:n.-270-3053_-270-3052insAATAGTGA
ENST00000682341.1:c.139-3053_139-3052insAATAGTGA ENSP00000508251.1:n.139-3053_139-3052insAATAGTGA
ENST00000682530.1:c.136-699_136-698insAATAGTGA ENSP00000506805.1:n.136-699_136-698insAATAGTGA
ENST00000682684.1:n.560-3053_560-3052insAATAGTGA
ENST00000683197.1:c.139-3053_139-3052insAATAGTGA ENSP00000507641.1:n.139-3053_139-3052insAATAGTGA
ENST00000683411.1:c.-270-3053_-270-3052insAATAGTGA ENSP00000508397.1:n.-270-3053_-270-3052insAATAGTGA
ENST00000683437.1:c.-270-3053_-270-3052insAATAGTGA ENSP00000508408.1:n.-270-3053_-270-3052insAATAGTGA
ENST00000683834.1:n.381-3053_381-3052insAATAGTGA
ENST00000683897.1:n.425-3053_425-3052insAATAGTGA
ENST00000684365.1:n.550-3053_550-3052insAATAGTGA
ENST00000684663.1:c.136-3053_136-3052insAATAGTGA ENSP00000508009.1:n.136-3053_136-3052insAATAGTGA
ENST00000324559.9:c.139-202_139-201insAATAGTGA MANE Select ENSP00000315371.9:n.139-202_139-201insAATAGTGA
ENST00000648804.1:n.670-542_670-541insAATAGTGA
ENST00000324559.8:c.139-202_139-201insAATAGTGA ENSP00000315371.8:n.139-202_139-201insAATAGTGA
NM_001142649.1:c.136-202_136-201insAATAGTGA NP_001136121.1:n.136-202_136-201insAATAGTGA
NM_213599.2:c.139-202_139-201insAATAGTGA , LRG_868t1:c.139-202_139-201insAATAGTGA NP_998764.1:n.139-202_139-201insAATAGTGA
XM_005252820.2:c.139-3053_139-3052insAATAGTGA XP_005252877.2:n.139-3053_139-3052insAATAGTGA
XM_005252821.2:c.136-3053_136-3052insAATAGTGA XP_005252878.2:n.136-3053_136-3052insAATAGTGA
XM_005252822.3:c.61-202_61-201insAATAGTGA XP_005252879.1:n.61-202_61-201insAATAGTGA
XM_005252823.3:c.58-202_58-201insAATAGTGA XP_005252880.1:n.58-202_58-201insAATAGTGA
XM_011519949.1:c.88-3053_88-3052insAATAGTGA XP_011518251.1:n.88-3053_88-3052insAATAGTGA
XM_005252820.3:c.139-3053_139-3052insAATAGTGA XP_005252877.2:n.139-3053_139-3052insAATAGTGA
XM_005252821.3:c.136-3053_136-3052insAATAGTGA XP_005252878.2:n.136-3053_136-3052insAATAGTGA
XM_005252822.4:c.61-202_61-201insAATAGTGA XP_005252879.1:n.61-202_61-201insAATAGTGA
XM_011519949.2:c.88-3053_88-3052insAATAGTGA XP_011518251.1:n.88-3053_88-3052insAATAGTGA
NM_001142649.2:c.136-202_136-201insAATAGTGA NP_001136121.1:n.136-202_136-201insAATAGTGA
NM_213599.3:c.139-202_139-201insAATAGTGA MANE Select NP_998764.1:n.139-202_139-201insAATAGTGA