Canonical Allele Identifier: CA1957403589
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22273246_22273249delinsAAAT , CM000673.2:g.22273246_22273249delinsAAAT GRCh38
NC_000011.9:g.22294792_22294795delinsAAAT , CM000673.1:g.22294792_22294795delinsAAAT GRCh37
NC_000011.8:g.22251368_22251371delinsAAAT NCBI36
NG_015844.1:g.85071_85074delinsAAAT , LRG_868:g.85071_85074delinsAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.252+257_252+260delinsAAAT
ENST00000682266.1:c.1785+257_1785+260delinsAAAT ENSP00000507766.1:n.1785+257_1785+260delinsAAAT
ENST00000682341.1:c.2193+257_2193+260delinsAAAT ENSP00000508251.1:n.2193+257_2193+260delinsAAAT
ENST00000683197.1:c.2193+257_2193+260delinsAAAT ENSP00000507641.1:n.2193+257_2193+260delinsAAAT
ENST00000683411.1:c.1785+257_1785+260delinsAAAT ENSP00000508397.1:n.1785+257_1785+260delinsAAAT
ENST00000683437.1:c.1785+257_1785+260delinsAAAT ENSP00000508408.1:n.1785+257_1785+260delinsAAAT
ENST00000683613.1:n.3229+257_3229+260delinsAAAT
ENST00000684663.1:c.2190+257_2190+260delinsAAAT ENSP00000508009.1:n.2190+257_2190+260delinsAAAT
ENST00000324559.9:c.2235+257_2235+260delinsAAAT MANE Select ENSP00000315371.9:n.2235+257_2235+260delinsAAAT
ENST00000648804.1:n.2570+257_2570+260delinsAAAT
ENST00000324559.8:c.2235+257_2235+260delinsAAAT ENSP00000315371.8:n.2235+257_2235+260delinsAAAT
ENST00000532043.1:n.252+257_252+260delinsAAAT
NM_001142649.1:c.2232+257_2232+260delinsAAAT NP_001136121.1:n.2232+257_2232+260delinsAAAT
NM_213599.2:c.2235+257_2235+260delinsAAAT , LRG_868t1:c.2235+257_2235+260delinsAAAT NP_998764.1:n.2235+257_2235+260delinsAAAT
XM_005252820.2:c.2193+257_2193+260delinsAAAT XP_005252877.2:n.2193+257_2193+260delinsAAAT
XM_005252821.2:c.2190+257_2190+260delinsAAAT XP_005252878.2:n.2190+257_2190+260delinsAAAT
XM_005252822.3:c.2157+257_2157+260delinsAAAT XP_005252879.1:n.2157+257_2157+260delinsAAAT
XM_005252823.3:c.2154+257_2154+260delinsAAAT XP_005252880.1:n.2154+257_2154+260delinsAAAT
XM_011519949.1:c.2142+257_2142+260delinsAAAT XP_011518251.1:n.2142+257_2142+260delinsAAAT
XM_005252820.3:c.2193+257_2193+260delinsAAAT XP_005252877.2:n.2193+257_2193+260delinsAAAT
XM_005252821.3:c.2190+257_2190+260delinsAAAT XP_005252878.2:n.2190+257_2190+260delinsAAAT
XM_005252822.4:c.2157+257_2157+260delinsAAAT XP_005252879.1:n.2157+257_2157+260delinsAAAT
XM_011519949.2:c.2142+257_2142+260delinsAAAT XP_011518251.1:n.2142+257_2142+260delinsAAAT
NM_001142649.2:c.2232+257_2232+260delinsAAAT NP_001136121.1:n.2232+257_2232+260delinsAAAT
NM_213599.3:c.2235+257_2235+260delinsAAAT MANE Select NP_998764.1:n.2235+257_2235+260delinsAAAT