Canonical Allele Identifier: CA598389487
Gene: ANO5 HGNC NCBI

Linked Data

dbSNP Id: rs764834668
MyVariant Identifiers: chr11:g.22294579del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22273038del , CM000673.2:g.22273038del GRCh38
NC_000011.9:g.22294584del , CM000673.1:g.22294584del GRCh37
NC_000011.8:g.22251160del NCBI36
NG_015844.1:g.84863del , LRG_868:g.84863del

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.252+49del
ENST00000682266.1:c.1785+49del ENSP00000507766.1:n.1785+49del
ENST00000682341.1:c.2193+49del ENSP00000508251.1:n.2193+49del
ENST00000683197.1:c.2193+49del ENSP00000507641.1:n.2193+49del
ENST00000683411.1:c.1785+49del ENSP00000508397.1:n.1785+49del
ENST00000683437.1:c.1785+49del ENSP00000508408.1:n.1785+49del
ENST00000683613.1:n.3229+49del
ENST00000684663.1:c.2190+49del ENSP00000508009.1:n.2190+49del
ENST00000324559.9:c.2235+49del MANE Select ENSP00000315371.9:n.2235+49del
ENST00000648804.1:n.2570+49del
ENST00000324559.8:c.2235+49del ENSP00000315371.8:n.2235+49del
ENST00000532043.1:n.252+49del
NM_001142649.1:c.2232+49del NP_001136121.1:n.2232+49del
NM_213599.2:c.2235+49del , LRG_868t1:c.2235+49del NP_998764.1:n.2235+49del
XM_005252820.2:c.2193+49del XP_005252877.2:n.2193+49del
XM_005252821.2:c.2190+49del XP_005252878.2:n.2190+49del
XM_005252822.3:c.2157+49del XP_005252879.1:n.2157+49del
XM_005252823.3:c.2154+49del XP_005252880.1:n.2154+49del
XM_011519949.1:c.2142+49del XP_011518251.1:n.2142+49del
XM_005252820.3:c.2193+49del XP_005252877.2:n.2193+49del
XM_005252821.3:c.2190+49del XP_005252878.2:n.2190+49del
XM_005252822.4:c.2157+49del XP_005252879.1:n.2157+49del
XM_011519949.2:c.2142+49del XP_011518251.1:n.2142+49del
NM_001142649.2:c.2232+49del NP_001136121.1:n.2232+49del
NM_213599.3:c.2235+49del MANE Select NP_998764.1:n.2235+49del