Canonical Allele Identifier: CA378879136
Gene: ANO9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.418804G>T , CM000673.2:g.418804G>T GRCh38
NC_000011.9:g.418804G>T , CM000673.1:g.418804G>T GRCh37
NC_000011.8:g.408804G>T NCBI36
NG_052610.1:g.28208C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332826.7:c.2046C>A MANE Select ENSP00000332788.6:p.Asp682Glu
ENST00000332826.6:c.2046C>A ENSP00000332788.6:p.Asp682Glu
ENST00000524802.1:n.538C>A
ENST00000526142.5:n.2127C>A
ENST00000528927.5:n.2157C>A
ENST00000532094.5:n.4751C>A
ENST00000534161.5:n.1419C>A
NM_001012302.2:c.2046C>A NP_001012302.2:p.Asp682Glu
XM_011520046.1:c.2040C>A XP_011518348.1:p.Asp680Glu
XM_011520049.1:c.1539C>A XP_011518351.1:p.Asp513Glu
XM_011520053.1:c.1149C>A XP_011518355.1:p.Asp383Glu
XR_428843.1:n.2102C>A
XR_428844.1:n.2019C>A
XR_930862.1:n.2213C>A
NM_001347882.1:c.1614C>A NP_001334811.1:p.Asp538Glu
XM_011520053.2:c.1149C>A XP_011518355.1:p.Asp383Glu
XR_001747846.1:n.2864C>A
XR_001747847.1:n.2858C>A
XR_001747848.1:n.2261C>A
XR_001747849.1:n.2868C>A
XR_001747850.1:n.3878C>A
XR_001747851.1:n.3897C>A
XR_001747852.1:n.2019C>A
XR_001747853.1:n.2960C>A
XR_001747854.1:n.1759C>A
XR_001747855.1:n.1646C>A
NM_001012302.3:c.2046C>A MANE Select NP_001012302.2:p.Asp682Glu
NM_001347882.2:c.1614C>A NP_001334811.1:p.Asp538Glu