Canonical Allele Identifier: CA10605384
Gene: ANO5 HGNC NCBI

Linked Data

ClinVar Variation Id: 286167
ClinVar RCV Id: RCV000481085
dbSNP Id: rs886043327

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22262117_22262127del , CM000673.2:g.22262117_22262127del GRCh38
NC_000011.9:g.22283663_22283673del , CM000673.1:g.22283663_22283673del GRCh37
NC_000011.8:g.22240239_22240249del NCBI36
NG_015844.1:g.73942_73952del , LRG_868:g.73942_73952del

Transcript Alleles

HGVS Amino-acid change
ENST00000682266.1:c.1181-12_1181-2del ENSP00000507766.1:n.1181-12_1181-2del
ENST00000682341.1:c.1589-12_1589-2del ENSP00000508251.1:n.1589-12_1589-2del
ENST00000683197.1:c.1589-12_1589-2del ENSP00000507641.1:n.1589-12_1589-2del
ENST00000683411.1:c.1181-12_1181-2del ENSP00000508397.1:n.1181-12_1181-2del
ENST00000683437.1:c.1181-12_1181-2del ENSP00000508408.1:n.1181-12_1181-2del
ENST00000683613.1:n.2625-12_2625-2del
ENST00000684663.1:c.1586-12_1586-2del ENSP00000508009.1:n.1586-12_1586-2del
ENST00000324559.9:c.1631-12_1631-2del MANE Select ENSP00000315371.9:n.1631-12_1631-2del
ENST00000648804.1:n.1966-12_1966-2del
ENST00000324559.8:c.1631-12_1631-2del ENSP00000315371.8:n.1631-12_1631-2del
NM_001142649.1:c.1628-12_1628-2del NP_001136121.1:n.1628-12_1628-2del
NM_213599.2:c.1631-12_1631-2del , LRG_868t1:c.1631-12_1631-2del NP_998764.1:n.1631-12_1631-2del
XM_005252820.2:c.1589-12_1589-2del XP_005252877.2:n.1589-12_1589-2del
XM_005252821.2:c.1586-12_1586-2del XP_005252878.2:n.1586-12_1586-2del
XM_005252822.3:c.1553-12_1553-2del XP_005252879.1:n.1553-12_1553-2del
XM_005252823.3:c.1550-12_1550-2del XP_005252880.1:n.1550-12_1550-2del
XM_011519949.1:c.1538-12_1538-2del XP_011518251.1:n.1538-12_1538-2del
XM_005252820.3:c.1589-12_1589-2del XP_005252877.2:n.1589-12_1589-2del
XM_005252821.3:c.1586-12_1586-2del XP_005252878.2:n.1586-12_1586-2del
XM_005252822.4:c.1553-12_1553-2del XP_005252879.1:n.1553-12_1553-2del
XM_011519949.2:c.1538-12_1538-2del XP_011518251.1:n.1538-12_1538-2del
NM_001142649.2:c.1628-12_1628-2del NP_001136121.1:n.1628-12_1628-2del
NM_213599.3:c.1631-12_1631-2del MANE Select NP_998764.1:n.1631-12_1631-2del