Canonical Allele Identifier: CA1957397384
Gene: ANO5 HGNC NCBI

Linked Data

dbSNP Id: rs1852809417

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22225867C>A , CM000673.2:g.22225867C>A GRCh38
NC_000011.9:g.22247413C>A , CM000673.1:g.22247413C>A GRCh37
NC_000011.8:g.22203989C>A NCBI36
NG_015844.1:g.37692C>A , LRG_868:g.37692C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682266.1:c.-156-117C>A ENSP00000507766.1:n.-156-117C>A
ENST00000682341.1:c.253-117C>A ENSP00000508251.1:n.253-117C>A
ENST00000682530.1:c.*227-117C>A ENSP00000506805.1:n.*227-117C>A
ENST00000682684.1:n.674-117C>A
ENST00000683197.1:c.253-117C>A ENSP00000507641.1:n.253-117C>A
ENST00000683411.1:c.-156-117C>A ENSP00000508397.1:n.-156-117C>A
ENST00000683437.1:c.-156-117C>A ENSP00000508408.1:n.-156-117C>A
ENST00000683613.1:n.1289-117C>A
ENST00000683834.1:n.495-117C>A
ENST00000684663.1:c.250-117C>A ENSP00000508009.1:n.250-117C>A
ENST00000324559.9:c.295-117C>A MANE Select ENSP00000315371.9:n.295-117C>A
ENST00000648804.1:n.860-117C>A
ENST00000324559.8:c.295-117C>A ENSP00000315371.8:n.295-117C>A
NM_001142649.1:c.292-117C>A NP_001136121.1:n.292-117C>A
NM_213599.2:c.295-117C>A , LRG_868t1:c.295-117C>A NP_998764.1:n.295-117C>A
XM_005252820.2:c.253-117C>A XP_005252877.2:n.253-117C>A
XM_005252821.2:c.250-117C>A XP_005252878.2:n.250-117C>A
XM_005252822.3:c.217-117C>A XP_005252879.1:n.217-117C>A
XM_005252823.3:c.214-117C>A XP_005252880.1:n.214-117C>A
XM_011519949.1:c.202-117C>A XP_011518251.1:n.202-117C>A
XM_005252820.3:c.253-117C>A XP_005252877.2:n.253-117C>A
XM_005252821.3:c.250-117C>A XP_005252878.2:n.250-117C>A
XM_005252822.4:c.217-117C>A XP_005252879.1:n.217-117C>A
XM_011519949.2:c.202-117C>A XP_011518251.1:n.202-117C>A
NM_001142649.2:c.292-117C>A NP_001136121.1:n.292-117C>A
NM_213599.3:c.295-117C>A MANE Select NP_998764.1:n.295-117C>A