Canonical Allele Identifier: CA2577566085

Gene: ANO10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43605714del , CM000665.2:g.43605714del	GRCh38
NC_000003.11:g.43647206del , CM000665.1:g.43647206del	GRCh37
NC_000003.10:g.43622210del	NCBI36
NG_028216.1:g.21356del
NG_028216.2:g.90882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292246.8:c.139+1del
ENST00000292246.7:c.139+1del
ENST00000350459.8:c.139+1del
ENST00000396091.7:c.139+1del
ENST00000413397.5:c.139+1del
ENST00000414522.6:c.139+1del
ENST00000427171.5:c.139+1del
ENST00000428472.5:c.139+1del
ENST00000428831.1:c.139+1del
ENST00000439141.5:c.139+1del
ENST00000444344.5:c.139+1del
ENST00000451430.6:c.139+1del
ENST00000456438.5:c.139+1del
NM_001204831.1:c.139+1del
NM_001204832.1:c.139+1del
NM_001204833.1:c.139+1del
NM_001204834.1:c.139+1del
NM_018075.3:c.139+1del
XM_011533882.1:c.139+1del
XM_011533883.1:c.139+1del
XM_011533884.1:c.139+1del
XM_011533885.1:c.139+1del
XM_011533886.1:c.139+1del
XM_011533887.1:c.139+1del
XM_011533888.1:c.139+1del
XM_011533889.1:c.139+1del
XM_011533890.1:c.139+1del
NM_001204831.2:c.139+1del
NM_001204832.2:c.139+1del
NM_001204833.2:c.139+1del
NM_001204834.2:c.139+1del
NM_001346463.1:c.139+1del
NM_001346464.1:c.139+1del
NM_001346465.1:c.139+1del
NM_001346466.1:c.139+1del
NM_001346467.1:c.139+1del
NM_001346468.1:c.139+1del
NM_001346469.1:c.139+1del
NM_018075.4:c.139+1del
XM_011533885.3:c.139+1del
XM_011533889.3:c.139+1del
XM_011533890.3:c.139+1del
XM_017006717.2:c.139+1del
XM_017006718.1:c.139+1del
XM_017006719.2:c.139+1del
XM_024453616.1:c.139+1del
XM_024453617.1:c.139+1del
XR_001740190.2:n.255+1del
NM_018075.5:c.139+1del
NM_001204831.3:c.139+1del
NM_001204832.3:c.139+1del
NM_001204833.3:c.139+1del
NM_001204834.3:c.139+1del
NM_001346463.2:c.139+1del
NM_001346464.2:c.139+1del
NM_001346465.2:c.139+1del
NM_001346466.2:c.139+1del
NM_001346467.2:c.139+1del
NM_001346468.2:c.139+1del
NM_001346469.2:c.139+1del