Canonical Allele Identifier: CA2612838591
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22263107_22263109del , CM000673.2:g.22263107_22263109del GRCh38
NC_000011.9:g.22284653_22284655del , CM000673.1:g.22284653_22284655del GRCh37
NC_000011.8:g.22241229_22241231del NCBI36
NG_015844.1:g.74932_74934del , LRG_868:g.74932_74934del

Transcript Alleles

HGVS Amino-acid change
ENST00000682266.1:c.1448+64_1448+66del ENSP00000507766.1:n.1448+64_1448+66del
ENST00000682341.1:c.1856+64_1856+66del ENSP00000508251.1:n.1856+64_1856+66del
ENST00000683197.1:c.1856+64_1856+66del ENSP00000507641.1:n.1856+64_1856+66del
ENST00000683411.1:c.1448+64_1448+66del ENSP00000508397.1:n.1448+64_1448+66del
ENST00000683437.1:c.1448+64_1448+66del ENSP00000508408.1:n.1448+64_1448+66del
ENST00000683613.1:n.2892+64_2892+66del
ENST00000684663.1:c.1853+64_1853+66del ENSP00000508009.1:n.1853+64_1853+66del
ENST00000324559.9:c.1898+64_1898+66del MANE Select ENSP00000315371.9:n.1898+64_1898+66del
ENST00000648804.1:n.2233+64_2233+66del
ENST00000324559.8:c.1898+64_1898+66del ENSP00000315371.8:n.1898+64_1898+66del
NM_001142649.1:c.1895+64_1895+66del NP_001136121.1:n.1895+64_1895+66del
NM_213599.2:c.1898+64_1898+66del , LRG_868t1:c.1898+64_1898+66del NP_998764.1:n.1898+64_1898+66del
XM_005252820.2:c.1856+64_1856+66del XP_005252877.2:n.1856+64_1856+66del
XM_005252821.2:c.1853+64_1853+66del XP_005252878.2:n.1853+64_1853+66del
XM_005252822.3:c.1820+64_1820+66del XP_005252879.1:n.1820+64_1820+66del
XM_005252823.3:c.1817+64_1817+66del XP_005252880.1:n.1817+64_1817+66del
XM_011519949.1:c.1805+64_1805+66del XP_011518251.1:n.1805+64_1805+66del
XM_005252820.3:c.1856+64_1856+66del XP_005252877.2:n.1856+64_1856+66del
XM_005252821.3:c.1853+64_1853+66del XP_005252878.2:n.1853+64_1853+66del
XM_005252822.4:c.1820+64_1820+66del XP_005252879.1:n.1820+64_1820+66del
XM_011519949.2:c.1805+64_1805+66del XP_011518251.1:n.1805+64_1805+66del
NM_001142649.2:c.1895+64_1895+66del NP_001136121.1:n.1895+64_1895+66del
NM_213599.3:c.1898+64_1898+66del MANE Select NP_998764.1:n.1898+64_1898+66del