Canonical Allele Identifier: CA10615867
Gene: ANO10 HGNC NCBI

Linked Data

ClinVar Variation Id: 345204
ClinVar RCV Id: RCV000367158
dbSNP Id: rs886058484
gnomAD v3: 3-43621999-G-T
gnomAD v4: 3-43621999-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43621999G>T , CM000665.2:g.43621999G>T GRCh38
NC_000003.11:g.43663491G>T , CM000665.1:g.43663491G>T GRCh37
NC_000003.10:g.43638495G>T NCBI36
NG_028216.1:g.5070C>A
NG_028216.2:g.74596C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292246.8:c.-102C>A MANE Select ENSP00000292246.3:n.-102C>A
ENST00000292246.7:c.-102C>A ENSP00000292246.3:n.-102C>A
ENST00000413397.5:c.-11-16136C>A ENSP00000399103.1:n.-11-16136C>A
ENST00000414522.6:c.-102C>A ENSP00000396990.2:n.-102C>A
ENST00000427171.5:c.-102C>A ENSP00000406432.1:n.-102C>A
ENST00000428472.5:c.-102C>A ENSP00000416266.1:n.-102C>A
ENST00000428831.1:c.-11-16136C>A ENSP00000406712.1:n.-11-16136C>A
ENST00000436073.1:c.-11-16136C>A ENSP00000404988.1:n.-11-16136C>A
ENST00000439141.5:c.-11-16136C>A ENSP00000397360.1:n.-11-16136C>A
ENST00000451430.6:c.-102C>A ENSP00000394119.2:n.-102C>A
NM_001204831.1:c.-102C>A NP_001191760.1:n.-102C>A
NM_001204832.1:c.-102C>A NP_001191761.1:n.-102C>A
NM_001204833.1:c.-102C>A NP_001191762.1:n.-102C>A
NM_001204834.1:c.-102C>A NP_001191763.1:n.-102C>A
NM_018075.3:c.-102C>A NP_060545.3:n.-102C>A
XM_011533882.1:c.-102C>A XP_011532184.1:n.-102C>A
XM_011533883.1:c.-11-16136C>A XP_011532185.1:n.-11-16136C>A
XM_011533884.1:c.-102C>A XP_011532186.1:n.-102C>A
XM_011533885.1:c.-102C>A XP_011532187.1:n.-102C>A
XM_011533886.1:c.-102C>A XP_011532188.1:n.-102C>A
XM_011533887.1:c.-102C>A XP_011532189.1:n.-102C>A
XM_011533889.1:c.-102C>A XP_011532191.1:n.-102C>A
XM_011533890.1:c.-102C>A XP_011532192.1:n.-102C>A
NM_001204831.2:c.-102C>A NP_001191760.1:n.-102C>A
NM_001204832.2:c.-102C>A NP_001191761.1:n.-102C>A
NM_001204833.2:c.-102C>A NP_001191762.1:n.-102C>A
NM_001204834.2:c.-102C>A NP_001191763.1:n.-102C>A
NM_001346463.1:c.-102C>A NP_001333392.1:n.-102C>A
NM_001346464.1:c.-102C>A NP_001333393.1:n.-102C>A
NM_001346465.1:c.-102C>A NP_001333394.1:n.-102C>A
NM_001346468.1:c.-11-16136C>A NP_001333397.1:n.-11-16136C>A
NM_001346469.1:c.-11-16136C>A NP_001333398.1:n.-11-16136C>A
NM_018075.4:c.-102C>A NP_060545.3:n.-102C>A
XM_011533885.3:c.-102C>A XP_011532187.2:n.-102C>A
XM_011533889.3:c.-102C>A XP_011532191.1:n.-102C>A
XM_011533890.3:c.-102C>A XP_011532192.1:n.-102C>A
XM_017006717.2:c.-11-16136C>A XP_016862206.1:n.-11-16136C>A
XM_017006718.1:c.-102C>A XP_016862207.1:n.-102C>A
XM_017006719.2:c.-102C>A XP_016862208.1:n.-102C>A
XM_024453616.1:c.-102C>A XP_024309384.1:n.-102C>A
XR_001740190.2:n.15C>A
NM_018075.5:c.-102C>A MANE Select NP_060545.3:n.-102C>A
NM_001204831.3:c.-102C>A NP_001191760.1:n.-102C>A
NM_001204832.3:c.-102C>A NP_001191761.1:n.-102C>A
NM_001204833.3:c.-102C>A NP_001191762.1:n.-102C>A
NM_001204834.3:c.-102C>A NP_001191763.1:n.-102C>A
NM_001346463.2:c.-102C>A NP_001333392.1:n.-102C>A
NM_001346464.2:c.-102C>A NP_001333393.1:n.-102C>A
NM_001346465.2:c.-102C>A NP_001333394.1:n.-102C>A
NM_001346466.2:c.-238C>A NP_001333395.1:n.-238C>A
NM_001346467.2:c.-238C>A NP_001333396.1:n.-238C>A
NM_001346468.2:c.-11-16136C>A NP_001333397.1:n.-11-16136C>A
NM_001346469.2:c.-11-16136C>A NP_001333398.1:n.-11-16136C>A