Canonical Allele Identifier: CA1957418676
Gene: ANO5 HGNC NCBI

Linked Data

dbSNP Id: rs1854113891

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22259451_22259452del , CM000673.2:g.22259451_22259452del GRCh38
NC_000011.9:g.22280997_22280998del , CM000673.1:g.22280997_22280998del GRCh37
NC_000011.8:g.22237573_22237574del NCBI36
NG_015844.1:g.71276_71277del , LRG_868:g.71276_71277del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682266.1:c.958-68_958-67del ENSP00000507766.1:n.958-68_958-67del
ENST00000682341.1:c.1366-68_1366-67del ENSP00000508251.1:n.1366-68_1366-67del
ENST00000683197.1:c.1366-68_1366-67del ENSP00000507641.1:n.1366-68_1366-67del
ENST00000683411.1:c.958-68_958-67del ENSP00000508397.1:n.958-68_958-67del
ENST00000683437.1:c.958-68_958-67del ENSP00000508408.1:n.958-68_958-67del
ENST00000683613.1:n.2402-68_2402-67del
ENST00000684663.1:c.1363-68_1363-67del ENSP00000508009.1:n.1363-68_1363-67del
ENST00000324559.9:c.1408-68_1408-67del MANE Select ENSP00000315371.9:n.1408-68_1408-67del
ENST00000648804.1:n.1743-68_1743-67del
ENST00000324559.8:c.1408-68_1408-67del ENSP00000315371.8:n.1408-68_1408-67del
NM_001142649.1:c.1405-68_1405-67del NP_001136121.1:n.1405-68_1405-67del
NM_213599.2:c.1408-68_1408-67del , LRG_868t1:c.1408-68_1408-67del NP_998764.1:n.1408-68_1408-67del
XM_005252820.2:c.1366-68_1366-67del XP_005252877.2:n.1366-68_1366-67del
XM_005252821.2:c.1363-68_1363-67del XP_005252878.2:n.1363-68_1363-67del
XM_005252822.3:c.1330-68_1330-67del XP_005252879.1:n.1330-68_1330-67del
XM_005252823.3:c.1327-68_1327-67del XP_005252880.1:n.1327-68_1327-67del
XM_011519949.1:c.1315-68_1315-67del XP_011518251.1:n.1315-68_1315-67del
XM_005252820.3:c.1366-68_1366-67del XP_005252877.2:n.1366-68_1366-67del
XM_005252821.3:c.1363-68_1363-67del XP_005252878.2:n.1363-68_1363-67del
XM_005252822.4:c.1330-68_1330-67del XP_005252879.1:n.1330-68_1330-67del
XM_011519949.2:c.1315-68_1315-67del XP_011518251.1:n.1315-68_1315-67del
NM_001142649.2:c.1405-68_1405-67del NP_001136121.1:n.1405-68_1405-67del
NM_213599.3:c.1408-68_1408-67del MANE Select NP_998764.1:n.1408-68_1408-67del