Canonical Allele Identifier: CA379922419
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22259728G>A , CM000673.2:g.22259728G>A GRCh38
NC_000011.9:g.22281274G>A , CM000673.1:g.22281274G>A GRCh37
NC_000011.8:g.22237850G>A NCBI36
NG_015844.1:g.71553G>A , LRG_868:g.71553G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682266.1:c.1167G>A ENSP00000507766.1:p.Trp389Ter
ENST00000682341.1:c.1575G>A ENSP00000508251.1:p.Trp525Ter
ENST00000683197.1:c.1575G>A ENSP00000507641.1:p.Trp525Ter
ENST00000683411.1:c.1167G>A ENSP00000508397.1:p.Trp389Ter
ENST00000683437.1:c.1167G>A ENSP00000508408.1:p.Trp389Ter
ENST00000683613.1:n.2611G>A
ENST00000684663.1:c.1572G>A ENSP00000508009.1:p.Trp524Ter
ENST00000324559.9:c.1617G>A MANE Select ENSP00000315371.9:p.Trp539Ter
ENST00000648804.1:n.1952G>A
ENST00000324559.8:c.1617G>A ENSP00000315371.8:p.Trp539Ter
NM_001142649.1:c.1614G>A NP_001136121.1:p.Trp538Ter
NM_213599.2:c.1617G>A , LRG_868t1:c.1617G>A NP_998764.1:p.Trp539Ter
XM_005252820.2:c.1575G>A XP_005252877.2:p.Trp525Ter
XM_005252821.2:c.1572G>A XP_005252878.2:p.Trp524Ter
XM_005252822.3:c.1539G>A XP_005252879.1:p.Trp513Ter
XM_005252823.3:c.1536G>A XP_005252880.1:p.Trp512Ter
XM_011519949.1:c.1524G>A XP_011518251.1:p.Trp508Ter
XM_005252820.3:c.1575G>A XP_005252877.2:p.Trp525Ter
XM_005252821.3:c.1572G>A XP_005252878.2:p.Trp524Ter
XM_005252822.4:c.1539G>A XP_005252879.1:p.Trp513Ter
XM_011519949.2:c.1524G>A XP_011518251.1:p.Trp508Ter
NM_001142649.2:c.1614G>A NP_001136121.1:p.Trp538Ter
NM_213599.3:c.1617G>A MANE Select NP_998764.1:p.Trp539Ter