Canonical Allele Identifier: CA1957393835
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22218088C= , CM000673.2:g.22218088C= GRCh38
NC_000011.9:g.22239634C= , CM000673.1:g.22239634C= GRCh37
NC_000011.8:g.22196210C= NCBI36
NG_015844.1:g.29913C= , LRG_868:g.29913C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682084.1:n.3313-158C=
ENST00000682266.1:c.-270-3009C= ENSP00000507766.1:n.-270-3009C=
ENST00000682341.1:c.139-3009C= ENSP00000508251.1:n.139-3009C=
ENST00000682530.1:c.136-655C= ENSP00000506805.1:n.136-655C=
ENST00000682684.1:n.560-3009C=
ENST00000683197.1:c.139-3009C= ENSP00000507641.1:n.139-3009C=
ENST00000683411.1:c.-270-3009C= ENSP00000508397.1:n.-270-3009C=
ENST00000683437.1:c.-270-3009C= ENSP00000508408.1:n.-270-3009C=
ENST00000683834.1:n.381-3009C=
ENST00000683897.1:n.425-3009C=
ENST00000684365.1:n.550-3009C=
ENST00000684663.1:c.136-3009C= ENSP00000508009.1:n.136-3009C=
ENST00000324559.9:c.139-158C= MANE Select ENSP00000315371.9:n.139-158C=
ENST00000648804.1:n.670-498C=
ENST00000324559.8:c.139-158C= ENSP00000315371.8:n.139-158C=
NM_001142649.1:c.136-158C= NP_001136121.1:n.136-158C=
NM_213599.2:c.139-158C= , LRG_868t1:c.139-158C= NP_998764.1:n.139-158C=
XM_005252820.2:c.139-3009C= XP_005252877.2:n.139-3009C=
XM_005252821.2:c.136-3009C= XP_005252878.2:n.136-3009C=
XM_005252822.3:c.61-158C= XP_005252879.1:n.61-158C=
XM_005252823.3:c.58-158C= XP_005252880.1:n.58-158C=
XM_011519949.1:c.88-3009C= XP_011518251.1:n.88-3009C=
XM_005252820.3:c.139-3009C= XP_005252877.2:n.139-3009C=
XM_005252821.3:c.136-3009C= XP_005252878.2:n.136-3009C=
XM_005252822.4:c.61-158C= XP_005252879.1:n.61-158C=
XM_011519949.2:c.88-3009C= XP_011518251.1:n.88-3009C=
NM_001142649.2:c.136-158C= NP_001136121.1:n.136-158C=
NM_213599.3:c.139-158C= MANE Select NP_998764.1:n.139-158C=