Canonical Allele Identifier: CA1957403175
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22272989_22272990delinsTG , CM000673.2:g.22272989_22272990delinsTG GRCh38
NC_000011.9:g.22294535_22294536delinsTG , CM000673.1:g.22294535_22294536delinsTG GRCh37
NC_000011.8:g.22251111_22251112delinsTG NCBI36
NG_015844.1:g.84814_84815delinsTG , LRG_868:g.84814_84815delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.252_252+1delinsTG
ENST00000682266.1:c.1785_1785+1delinsTG
ENST00000682341.1:c.2193_2193+1delinsTG
ENST00000683197.1:c.2193_2193+1delinsTG
ENST00000683411.1:c.1785_1785+1delinsTG
ENST00000683437.1:c.1785_1785+1delinsTG
ENST00000683613.1:n.3229_3229+1delinsTG
ENST00000684663.1:c.2190_2190+1delinsTG
ENST00000324559.9:c.2235_2235+1delinsTG
ENST00000648804.1:n.2570_2570+1delinsTG
ENST00000324559.8:c.2235_2235+1delinsTG
ENST00000532043.1:n.252_252+1delinsTG
NM_001142649.1:c.2232_2232+1delinsTG
NM_213599.2:c.2235_2235+1delinsTG , LRG_868t1:c.2235_2235+1delinsTG
XM_005252820.2:c.2193_2193+1delinsTG
XM_005252821.2:c.2190_2190+1delinsTG
XM_005252822.3:c.2157_2157+1delinsTG
XM_005252823.3:c.2154_2154+1delinsTG
XM_011519949.1:c.2142_2142+1delinsTG
XM_005252820.3:c.2193_2193+1delinsTG
XM_005252821.3:c.2190_2190+1delinsTG
XM_005252822.4:c.2157_2157+1delinsTG
XM_011519949.2:c.2142_2142+1delinsTG
NM_001142649.2:c.2232_2232+1delinsTG
NM_213599.3:c.2235_2235+1delinsTG