Canonical Allele Identifier: CA2341138
Gene: ANO10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1323907
dbSNP Id: rs777450156
gnomAD v2: 3-43647205-C-A
gnomAD v3: 3-43605713-C-A
gnomAD v4: 3-43605713-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43605713C>A , CM000665.2:g.43605713C>A GRCh38
NC_000003.11:g.43647205C>A , CM000665.1:g.43647205C>A GRCh37
NC_000003.10:g.43622209C>A NCBI36
NG_028216.1:g.21356G>T
NG_028216.2:g.90882G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292246.8:c.139+1G>T MANE Select ENSP00000292246.3:n.139+1G>T
ENST00000292246.7:c.139+1G>T ENSP00000292246.3:n.139+1G>T
ENST00000350459.8:c.139+1G>T ENSP00000327767.4:n.139+1G>T
ENST00000396091.7:c.139+1G>T ENSP00000379398.3:n.139+1G>T
ENST00000413397.5:c.139+1G>T ENSP00000399103.1:n.139+1G>T
ENST00000414522.6:c.139+1G>T ENSP00000396990.2:n.139+1G>T
ENST00000427171.5:c.139+1G>T ENSP00000406432.1:n.139+1G>T
ENST00000428472.5:c.139+1G>T ENSP00000416266.1:n.139+1G>T
ENST00000428831.1:c.139+1G>T ENSP00000406712.1:n.139+1G>T
ENST00000439141.5:c.139+1G>T ENSP00000397360.1:n.139+1G>T
ENST00000444344.5:c.139+1G>T ENSP00000402010.1:n.139+1G>T
ENST00000451430.6:c.139+1G>T ENSP00000394119.2:n.139+1G>T
ENST00000456438.5:c.139+1G>T ENSP00000402845.1:n.139+1G>T
NM_001204831.1:c.139+1G>T NP_001191760.1:n.139+1G>T
NM_001204832.1:c.139+1G>T NP_001191761.1:n.139+1G>T
NM_001204833.1:c.139+1G>T NP_001191762.1:n.139+1G>T
NM_001204834.1:c.139+1G>T NP_001191763.1:n.139+1G>T
NM_018075.3:c.139+1G>T NP_060545.3:n.139+1G>T
XM_011533882.1:c.139+1G>T XP_011532184.1:n.139+1G>T
XM_011533883.1:c.139+1G>T XP_011532185.1:n.139+1G>T
XM_011533884.1:c.139+1G>T XP_011532186.1:n.139+1G>T
XM_011533885.1:c.139+1G>T XP_011532187.1:n.139+1G>T
XM_011533886.1:c.139+1G>T XP_011532188.1:n.139+1G>T
XM_011533887.1:c.139+1G>T XP_011532189.1:n.139+1G>T
XM_011533888.1:c.139+1G>T XP_011532190.1:n.139+1G>T
XM_011533889.1:c.139+1G>T XP_011532191.1:n.139+1G>T
XM_011533890.1:c.139+1G>T XP_011532192.1:n.139+1G>T
NM_001204831.2:c.139+1G>T NP_001191760.1:n.139+1G>T
NM_001204832.2:c.139+1G>T NP_001191761.1:n.139+1G>T
NM_001204833.2:c.139+1G>T NP_001191762.1:n.139+1G>T
NM_001204834.2:c.139+1G>T NP_001191763.1:n.139+1G>T
NM_001346463.1:c.139+1G>T NP_001333392.1:n.139+1G>T
NM_001346464.1:c.139+1G>T NP_001333393.1:n.139+1G>T
NM_001346465.1:c.139+1G>T NP_001333394.1:n.139+1G>T
NM_001346466.1:c.139+1G>T NP_001333395.1:n.139+1G>T
NM_001346467.1:c.139+1G>T NP_001333396.1:n.139+1G>T
NM_001346468.1:c.139+1G>T NP_001333397.1:n.139+1G>T
NM_001346469.1:c.139+1G>T NP_001333398.1:n.139+1G>T
NM_018075.4:c.139+1G>T NP_060545.3:n.139+1G>T
XM_011533885.3:c.139+1G>T XP_011532187.2:n.139+1G>T
XM_011533889.3:c.139+1G>T XP_011532191.1:n.139+1G>T
XM_011533890.3:c.139+1G>T XP_011532192.1:n.139+1G>T
XM_017006717.2:c.139+1G>T XP_016862206.1:n.139+1G>T
XM_017006718.1:c.139+1G>T XP_016862207.1:n.139+1G>T
XM_017006719.2:c.139+1G>T XP_016862208.1:n.139+1G>T
XM_024453616.1:c.139+1G>T XP_024309384.1:n.139+1G>T
XM_024453617.1:c.139+1G>T XP_024309385.1:n.139+1G>T
XR_001740190.2:n.255+1G>T
NM_018075.5:c.139+1G>T MANE Select NP_060545.3:n.139+1G>T
NM_001204831.3:c.139+1G>T NP_001191760.1:n.139+1G>T
NM_001204832.3:c.139+1G>T NP_001191761.1:n.139+1G>T
NM_001204833.3:c.139+1G>T NP_001191762.1:n.139+1G>T
NM_001204834.3:c.139+1G>T NP_001191763.1:n.139+1G>T
NM_001346463.2:c.139+1G>T NP_001333392.1:n.139+1G>T
NM_001346464.2:c.139+1G>T NP_001333393.1:n.139+1G>T
NM_001346465.2:c.139+1G>T NP_001333394.1:n.139+1G>T
NM_001346466.2:c.139+1G>T NP_001333395.1:n.139+1G>T
NM_001346467.2:c.139+1G>T NP_001333396.1:n.139+1G>T
NM_001346468.2:c.139+1G>T NP_001333397.1:n.139+1G>T
NM_001346469.2:c.139+1G>T NP_001333398.1:n.139+1G>T