Canonical Allele Identifier: CA1957393896
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22218161G= , CM000673.2:g.22218161G= GRCh38
NC_000011.9:g.22239707G= , CM000673.1:g.22239707G= GRCh37
NC_000011.8:g.22196283G= NCBI36
NG_015844.1:g.29986G= , LRG_868:g.29986G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682084.1:n.3313-85G=
ENST00000682266.1:c.-270-2936G= ENSP00000507766.1:n.-270-2936G=
ENST00000682341.1:c.139-2936G= ENSP00000508251.1:n.139-2936G=
ENST00000682530.1:c.136-582G= ENSP00000506805.1:n.136-582G=
ENST00000682684.1:n.560-2936G=
ENST00000683197.1:c.139-2936G= ENSP00000507641.1:n.139-2936G=
ENST00000683411.1:c.-270-2936G= ENSP00000508397.1:n.-270-2936G=
ENST00000683437.1:c.-270-2936G= ENSP00000508408.1:n.-270-2936G=
ENST00000683834.1:n.381-2936G=
ENST00000683897.1:n.425-2936G=
ENST00000684365.1:n.550-2936G=
ENST00000684663.1:c.136-2936G= ENSP00000508009.1:n.136-2936G=
ENST00000324559.9:c.139-85G= MANE Select ENSP00000315371.9:n.139-85G=
ENST00000648804.1:n.670-425G=
ENST00000324559.8:c.139-85G= ENSP00000315371.8:n.139-85G=
NM_001142649.1:c.136-85G= NP_001136121.1:n.136-85G=
NM_213599.2:c.139-85G= , LRG_868t1:c.139-85G= NP_998764.1:n.139-85G=
XM_005252820.2:c.139-2936G= XP_005252877.2:n.139-2936G=
XM_005252821.2:c.136-2936G= XP_005252878.2:n.136-2936G=
XM_005252822.3:c.61-85G= XP_005252879.1:n.61-85G=
XM_005252823.3:c.58-85G= XP_005252880.1:n.58-85G=
XM_011519949.1:c.88-2936G= XP_011518251.1:n.88-2936G=
XM_005252820.3:c.139-2936G= XP_005252877.2:n.139-2936G=
XM_005252821.3:c.136-2936G= XP_005252878.2:n.136-2936G=
XM_005252822.4:c.61-85G= XP_005252879.1:n.61-85G=
XM_011519949.2:c.88-2936G= XP_011518251.1:n.88-2936G=
NM_001142649.2:c.136-85G= NP_001136121.1:n.136-85G=
NM_213599.3:c.139-85G= MANE Select NP_998764.1:n.139-85G=