Canonical Allele Identifier: CA379923970
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22272945C>A , CM000673.2:g.22272945C>A GRCh38
NC_000011.9:g.22294491C>A , CM000673.1:g.22294491C>A GRCh37
NC_000011.8:g.22251067C>A NCBI36
NG_015844.1:g.84770C>A , LRG_868:g.84770C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.208C>A
ENST00000682266.1:c.1741C>A ENSP00000507766.1:p.Gln581Lys
ENST00000682341.1:c.2149C>A ENSP00000508251.1:p.Gln717Lys
ENST00000683197.1:c.2149C>A ENSP00000507641.1:p.Gln717Lys
ENST00000683411.1:c.1741C>A ENSP00000508397.1:p.Gln581Lys
ENST00000683437.1:c.1741C>A ENSP00000508408.1:p.Gln581Lys
ENST00000683613.1:n.3185C>A
ENST00000684663.1:c.2146C>A ENSP00000508009.1:p.Gln716Lys
ENST00000324559.9:c.2191C>A MANE Select ENSP00000315371.9:p.Gln731Lys
ENST00000648804.1:n.2526C>A
ENST00000324559.8:c.2191C>A ENSP00000315371.8:p.Gln731Lys
ENST00000532043.1:n.208C>A
NM_001142649.1:c.2188C>A NP_001136121.1:p.Gln730Lys
NM_213599.2:c.2191C>A , LRG_868t1:c.2191C>A NP_998764.1:p.Gln731Lys
XM_005252820.2:c.2149C>A XP_005252877.2:p.Gln717Lys
XM_005252821.2:c.2146C>A XP_005252878.2:p.Gln716Lys
XM_005252822.3:c.2113C>A XP_005252879.1:p.Gln705Lys
XM_005252823.3:c.2110C>A XP_005252880.1:p.Gln704Lys
XM_011519949.1:c.2098C>A XP_011518251.1:p.Gln700Lys
XM_005252820.3:c.2149C>A XP_005252877.2:p.Gln717Lys
XM_005252821.3:c.2146C>A XP_005252878.2:p.Gln716Lys
XM_005252822.4:c.2113C>A XP_005252879.1:p.Gln705Lys
XM_011519949.2:c.2098C>A XP_011518251.1:p.Gln700Lys
NM_001142649.2:c.2188C>A NP_001136121.1:p.Gln730Lys
NM_213599.3:c.2191C>A MANE Select NP_998764.1:p.Gln731Lys