Canonical Allele Identifier: CA1957420229
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22263053_22263061delinsACTTACAAG , CM000673.2:g.22263053_22263061delinsACTTACAAG GRCh38
NC_000011.9:g.22284599_22284607delinsACTTACAAG , CM000673.1:g.22284599_22284607delinsACTTACAAG GRCh37
NC_000011.8:g.22241175_22241183delinsACTTACAAG NCBI36
NG_015844.1:g.74878_74886delinsACTTACAAG , LRG_868:g.74878_74886delinsACTTACAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000682266.1:c.1448+10_1448+18delinsACTTACAAG ENSP00000507766.1:n.1448+10_1448+18delins...
ENST00000682341.1:c.1856+10_1856+18delinsACTTACAAG ENSP00000508251.1:n.1856+10_1856+18delins...
ENST00000683197.1:c.1856+10_1856+18delinsACTTACAAG ENSP00000507641.1:n.1856+10_1856+18delins...
ENST00000683411.1:c.1448+10_1448+18delinsACTTACAAG ENSP00000508397.1:n.1448+10_1448+18delins...
ENST00000683437.1:c.1448+10_1448+18delinsACTTACAAG ENSP00000508408.1:n.1448+10_1448+18delins...
ENST00000683613.1:n.2892+10_2892+18delinsACTTACAAG
ENST00000684663.1:c.1853+10_1853+18delinsACTTACAAG ENSP00000508009.1:n.1853+10_1853+18delins...
ENST00000324559.9:c.1898+10_1898+18delinsACTTACAAG MANE Select ENSP00000315371.9:n.1898+10_1898+18delins...
ENST00000648804.1:n.2233+10_2233+18delinsACTTACAAG
ENST00000324559.8:c.1898+10_1898+18delinsACTTACAAG ENSP00000315371.8:n.1898+10_1898+18delins...
NM_001142649.1:c.1895+10_1895+18delinsACTTACAAG NP_001136121.1:n.1895+10_1895+18delinsACT...
NM_213599.2:c.1898+10_1898+18delinsACTTACAAG , LRG_868t1:c.1898+10_1898+18delinsACTTACAAG NP_998764.1:n.1898+10_1898+18delinsACTTAC...
XM_005252820.2:c.1856+10_1856+18delinsACTTACAAG XP_005252877.2:n.1856+10_1856+18delinsACT...
XM_005252821.2:c.1853+10_1853+18delinsACTTACAAG XP_005252878.2:n.1853+10_1853+18delinsACT...
XM_005252822.3:c.1820+10_1820+18delinsACTTACAAG XP_005252879.1:n.1820+10_1820+18delinsACT...
XM_005252823.3:c.1817+10_1817+18delinsACTTACAAG XP_005252880.1:n.1817+10_1817+18delinsACT...
XM_011519949.1:c.1805+10_1805+18delinsACTTACAAG XP_011518251.1:n.1805+10_1805+18delinsACT...
XM_005252820.3:c.1856+10_1856+18delinsACTTACAAG XP_005252877.2:n.1856+10_1856+18delinsACT...
XM_005252821.3:c.1853+10_1853+18delinsACTTACAAG XP_005252878.2:n.1853+10_1853+18delinsACT...
XM_005252822.4:c.1820+10_1820+18delinsACTTACAAG XP_005252879.1:n.1820+10_1820+18delinsACT...
XM_011519949.2:c.1805+10_1805+18delinsACTTACAAG XP_011518251.1:n.1805+10_1805+18delinsACT...
NM_001142649.2:c.1895+10_1895+18delinsACTTACAAG NP_001136121.1:n.1895+10_1895+18delinsACT...
NM_213599.3:c.1898+10_1898+18delinsACTTACAAG MANE Select NP_998764.1:n.1898+10_1898+18delinsACTTAC...