Canonical Allele Identifier: CA5777477
Gene: ANO9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.429659C>G , CM000673.2:g.429659C>G GRCh38
NC_000011.9:g.429659C>G , CM000673.1:g.429659C>G GRCh37
NC_000011.8:g.419659C>G NCBI36
NG_052610.1:g.17353G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332826.7:c.833-7G>C MANE Select ENSP00000332788.6:n.833-7G>C
ENST00000332826.6:c.833-7G>C ENSP00000332788.6:n.833-7G>C
ENST00000525857.1:n.357-7G>C
ENST00000526142.5:n.100G>C
ENST00000528927.5:n.944-7G>C
ENST00000532094.5:n.2696G>C
ENST00000534161.5:n.110-7G>C
NM_001012302.2:c.833-7G>C NP_001012302.2:n.833-7G>C
XM_011520046.1:c.827-7G>C XP_011518348.1:n.827-7G>C
XM_011520047.1:c.833-7G>C XP_011518349.1:n.833-7G>C
XM_011520048.1:c.833-7G>C XP_011518350.1:n.833-7G>C
XM_011520049.1:c.326-7G>C XP_011518351.1:n.326-7G>C
XM_011520050.1:c.833-7G>C XP_011518352.1:n.833-7G>C
XM_011520051.1:c.833-7G>C XP_011518353.1:n.833-7G>C
XM_011520052.1:c.833-7G>C XP_011518354.1:n.833-7G>C
XM_011520053.1:c.-161-7G>C XP_011518355.1:n.-161-7G>C
XR_428843.1:n.918-7G>C
XR_428844.1:n.918-7G>C
XR_930862.1:n.918-7G>C
XR_930863.1:n.918-7G>C
NM_001347882.1:c.401-7G>C NP_001334811.1:n.401-7G>C
XM_011520051.2:c.833-7G>C XP_011518353.1:n.833-7G>C
XM_011520052.2:c.833-7G>C XP_011518354.1:n.833-7G>C
XM_011520053.2:c.-161-7G>C XP_011518355.1:n.-161-7G>C
XM_017017644.1:c.833-7G>C XP_016873133.1:n.833-7G>C
XM_017017645.1:c.833-7G>C XP_016873134.1:n.833-7G>C
XM_017017646.1:c.833-7G>C XP_016873135.1:n.833-7G>C
XM_017017647.1:c.833-7G>C XP_016873136.1:n.833-7G>C
XR_001747846.1:n.918-7G>C
XR_001747847.1:n.912-7G>C
XR_001747848.1:n.918-7G>C
XR_001747849.1:n.922-7G>C
XR_001747850.1:n.918-7G>C
XR_001747851.1:n.918-7G>C
XR_001747852.1:n.918-7G>C
XR_001747853.1:n.918-7G>C
NM_001012302.3:c.833-7G>C MANE Select NP_001012302.2:n.833-7G>C
NM_001347882.2:c.401-7G>C NP_001334811.1:n.401-7G>C