Canonical Allele Identifier: CA2612836973
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22255331_22255339del , CM000673.2:g.22255331_22255339del GRCh38
NC_000011.9:g.22276877_22276885del , CM000673.1:g.22276877_22276885del GRCh37
NC_000011.8:g.22233453_22233461del NCBI36
NG_015844.1:g.67156_67164del , LRG_868:g.67156_67164del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682089.1:n.501-40_501-32del
ENST00000682266.1:c.731-40_731-32del ENSP00000507766.1:n.731-40_731-32del
ENST00000682341.1:c.1139-40_1139-32del ENSP00000508251.1:n.1139-40_1139-32del
ENST00000682530.1:c.*1113-40_*1113-32del ENSP00000506805.1:n.*1113-40_*1113-32del
ENST00000683197.1:c.1139-40_1139-32del ENSP00000507641.1:n.1139-40_1139-32del
ENST00000683411.1:c.731-40_731-32del ENSP00000508397.1:n.731-40_731-32del
ENST00000683437.1:c.731-40_731-32del ENSP00000508408.1:n.731-40_731-32del
ENST00000683613.1:n.2175-40_2175-32del
ENST00000683834.1:n.1381-40_1381-32del
ENST00000684663.1:c.1136-40_1136-32del ENSP00000508009.1:n.1136-40_1136-32del
ENST00000324559.9:c.1181-40_1181-32del MANE Select ENSP00000315371.9:n.1181-40_1181-32del
ENST00000648804.1:n.1516-40_1516-32del
ENST00000324559.8:c.1181-40_1181-32del ENSP00000315371.8:n.1181-40_1181-32del
NM_001142649.1:c.1178-40_1178-32del NP_001136121.1:n.1178-40_1178-32del
NM_213599.2:c.1181-40_1181-32del , LRG_868t1:c.1181-40_1181-32del NP_998764.1:n.1181-40_1181-32del
XM_005252820.2:c.1139-40_1139-32del XP_005252877.2:n.1139-40_1139-32del
XM_005252821.2:c.1136-40_1136-32del XP_005252878.2:n.1136-40_1136-32del
XM_005252822.3:c.1103-40_1103-32del XP_005252879.1:n.1103-40_1103-32del
XM_005252823.3:c.1100-40_1100-32del XP_005252880.1:n.1100-40_1100-32del
XM_011519949.1:c.1088-40_1088-32del XP_011518251.1:n.1088-40_1088-32del
XM_005252820.3:c.1139-40_1139-32del XP_005252877.2:n.1139-40_1139-32del
XM_005252821.3:c.1136-40_1136-32del XP_005252878.2:n.1136-40_1136-32del
XM_005252822.4:c.1103-40_1103-32del XP_005252879.1:n.1103-40_1103-32del
XM_011519949.2:c.1088-40_1088-32del XP_011518251.1:n.1088-40_1088-32del
NM_001142649.2:c.1178-40_1178-32del NP_001136121.1:n.1178-40_1178-32del
NM_213599.3:c.1181-40_1181-32del MANE Select NP_998764.1:n.1181-40_1181-32del