Canonical Allele Identifier: CA379922656
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22262212T>A , CM000673.2:g.22262212T>A GRCh38
NC_000011.9:g.22283758T>A , CM000673.1:g.22283758T>A GRCh37
NC_000011.8:g.22240334T>A NCBI36
NG_015844.1:g.74037T>A , LRG_868:g.74037T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682266.1:c.1264T>A ENSP00000507766.1:p.Cys422Ser
ENST00000682341.1:c.1672T>A ENSP00000508251.1:p.Cys558Ser
ENST00000683197.1:c.1672T>A ENSP00000507641.1:p.Cys558Ser
ENST00000683411.1:c.1264T>A ENSP00000508397.1:p.Cys422Ser
ENST00000683437.1:c.1264T>A ENSP00000508408.1:p.Cys422Ser
ENST00000683613.1:n.2708T>A
ENST00000684663.1:c.1669T>A ENSP00000508009.1:p.Cys557Ser
ENST00000324559.9:c.1714T>A MANE Select ENSP00000315371.9:p.Cys572Ser
ENST00000648804.1:n.2049T>A
ENST00000324559.8:c.1714T>A ENSP00000315371.8:p.Cys572Ser
NM_001142649.1:c.1711T>A NP_001136121.1:p.Cys571Ser
NM_213599.2:c.1714T>A , LRG_868t1:c.1714T>A NP_998764.1:p.Cys572Ser
XM_005252820.2:c.1672T>A XP_005252877.2:p.Cys558Ser
XM_005252821.2:c.1669T>A XP_005252878.2:p.Cys557Ser
XM_005252822.3:c.1636T>A XP_005252879.1:p.Cys546Ser
XM_005252823.3:c.1633T>A XP_005252880.1:p.Cys545Ser
XM_011519949.1:c.1621T>A XP_011518251.1:p.Cys541Ser
XM_005252820.3:c.1672T>A XP_005252877.2:p.Cys558Ser
XM_005252821.3:c.1669T>A XP_005252878.2:p.Cys557Ser
XM_005252822.4:c.1636T>A XP_005252879.1:p.Cys546Ser
XM_011519949.2:c.1621T>A XP_011518251.1:p.Cys541Ser
NM_001142649.2:c.1711T>A NP_001136121.1:p.Cys571Ser
NM_213599.3:c.1714T>A MANE Select NP_998764.1:p.Cys572Ser