Canonical Allele Identifier: CA242118
Gene: ANO5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22276182_22276184del , CM000673.2:g.22276182_22276184del GRCh38
NC_000011.9:g.22297728_22297730del , CM000673.1:g.22297728_22297730del GRCh37
NC_000011.8:g.22254304_22254306del NCBI36
NG_015844.1:g.88007_88009del , LRG_868:g.88007_88009del

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.520_522del
ENST00000682266.1:c.2053_2055del ENSP00000507766.1:p.Phe685del
ENST00000682341.1:c.2461_2463del ENSP00000508251.1:p.Phe821del
ENST00000683197.1:c.2372+1435_2372+1437del ENSP00000507641.1:n.2372+1435_2372+1437del
ENST00000683411.1:c.2053_2055del ENSP00000508397.1:p.Phe685del
ENST00000683437.1:c.2053_2055del ENSP00000508408.1:p.Phe685del
ENST00000683613.1:n.3497_3499del
ENST00000684663.1:c.2458_2460del ENSP00000508009.1:p.Phe820del
ENST00000324559.9:c.2503_2505del MANE Select ENSP00000315371.9:p.Phe835del
ENST00000648804.1:n.2838_2840del
ENST00000324559.8:c.2503_2505del ENSP00000315371.8:p.Phe835del
ENST00000532043.1:n.520_522del
NM_001142649.1:c.2500_2502del NP_001136121.1:p.Phe834del
NM_213599.2:c.2503_2505del , LRG_868t1:c.2503_2505del NP_998764.1:p.Phe835del
XM_005252820.2:c.2461_2463del XP_005252877.2:p.Phe821del
XM_005252821.2:c.2458_2460del XP_005252878.2:p.Phe820del
XM_005252822.3:c.2425_2427del XP_005252879.1:p.Phe809del
XM_005252823.3:c.2422_2424del XP_005252880.1:p.Phe808del
XM_011519949.1:c.2410_2412del XP_011518251.1:p.Phe804del
XM_005252820.3:c.2461_2463del XP_005252877.2:p.Phe821del
XM_005252821.3:c.2458_2460del XP_005252878.2:p.Phe820del
XM_005252822.4:c.2425_2427del XP_005252879.1:p.Phe809del
XM_011519949.2:c.2410_2412del XP_011518251.1:p.Phe804del
NM_001142649.2:c.2500_2502del NP_001136121.1:p.Phe834del
NM_213599.3:c.2503_2505del MANE Select NP_998764.1:p.Phe835del
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