Canonical Allele Identifier: CA379922291
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22259671C>A , CM000673.2:g.22259671C>A GRCh38
NC_000011.9:g.22281217C>A , CM000673.1:g.22281217C>A GRCh37
NC_000011.8:g.22237793C>A NCBI36
NG_015844.1:g.71496C>A , LRG_868:g.71496C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682266.1:c.1110C>A ENSP00000507766.1:p.Cys370Ter
ENST00000682341.1:c.1518C>A ENSP00000508251.1:p.Cys506Ter
ENST00000683197.1:c.1518C>A ENSP00000507641.1:p.Cys506Ter
ENST00000683411.1:c.1110C>A ENSP00000508397.1:p.Cys370Ter
ENST00000683437.1:c.1110C>A ENSP00000508408.1:p.Cys370Ter
ENST00000683613.1:n.2554C>A
ENST00000684663.1:c.1515C>A ENSP00000508009.1:p.Cys505Ter
ENST00000324559.9:c.1560C>A MANE Select ENSP00000315371.9:p.Cys520Ter
ENST00000648804.1:n.1895C>A
ENST00000324559.8:c.1560C>A ENSP00000315371.8:p.Cys520Ter
NM_001142649.1:c.1557C>A NP_001136121.1:p.Cys519Ter
NM_213599.2:c.1560C>A , LRG_868t1:c.1560C>A NP_998764.1:p.Cys520Ter
XM_005252820.2:c.1518C>A XP_005252877.2:p.Cys506Ter
XM_005252821.2:c.1515C>A XP_005252878.2:p.Cys505Ter
XM_005252822.3:c.1482C>A XP_005252879.1:p.Cys494Ter
XM_005252823.3:c.1479C>A XP_005252880.1:p.Cys493Ter
XM_011519949.1:c.1467C>A XP_011518251.1:p.Cys489Ter
XM_005252820.3:c.1518C>A XP_005252877.2:p.Cys506Ter
XM_005252821.3:c.1515C>A XP_005252878.2:p.Cys505Ter
XM_005252822.4:c.1482C>A XP_005252879.1:p.Cys494Ter
XM_011519949.2:c.1467C>A XP_011518251.1:p.Cys489Ter
NM_001142649.2:c.1557C>A NP_001136121.1:p.Cys519Ter
NM_213599.3:c.1560C>A MANE Select NP_998764.1:p.Cys520Ter