Canonical Allele Identifier: CA1957393805
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22218036T= , CM000673.2:g.22218036T= GRCh38
NC_000011.9:g.22239582T= , CM000673.1:g.22239582T= GRCh37
NC_000011.8:g.22196158T= NCBI36
NG_015844.1:g.29861T= , LRG_868:g.29861T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682084.1:n.3313-210T=
ENST00000682266.1:c.-270-3061T= ENSP00000507766.1:n.-270-3061T=
ENST00000682341.1:c.139-3061T= ENSP00000508251.1:n.139-3061T=
ENST00000682530.1:c.136-707T= ENSP00000506805.1:n.136-707T=
ENST00000682684.1:n.560-3061T=
ENST00000683197.1:c.139-3061T= ENSP00000507641.1:n.139-3061T=
ENST00000683411.1:c.-270-3061T= ENSP00000508397.1:n.-270-3061T=
ENST00000683437.1:c.-270-3061T= ENSP00000508408.1:n.-270-3061T=
ENST00000683834.1:n.381-3061T=
ENST00000683897.1:n.425-3061T=
ENST00000684365.1:n.550-3061T=
ENST00000684663.1:c.136-3061T= ENSP00000508009.1:n.136-3061T=
ENST00000324559.9:c.139-210T= MANE Select ENSP00000315371.9:n.139-210T=
ENST00000648804.1:n.670-550T=
ENST00000324559.8:c.139-210T= ENSP00000315371.8:n.139-210T=
NM_001142649.1:c.136-210T= NP_001136121.1:n.136-210T=
NM_213599.2:c.139-210T= , LRG_868t1:c.139-210T= NP_998764.1:n.139-210T=
XM_005252820.2:c.139-3061T= XP_005252877.2:n.139-3061T=
XM_005252821.2:c.136-3061T= XP_005252878.2:n.136-3061T=
XM_005252822.3:c.61-210T= XP_005252879.1:n.61-210T=
XM_005252823.3:c.58-210T= XP_005252880.1:n.58-210T=
XM_011519949.1:c.88-3061T= XP_011518251.1:n.88-3061T=
XM_005252820.3:c.139-3061T= XP_005252877.2:n.139-3061T=
XM_005252821.3:c.136-3061T= XP_005252878.2:n.136-3061T=
XM_005252822.4:c.61-210T= XP_005252879.1:n.61-210T=
XM_011519949.2:c.88-3061T= XP_011518251.1:n.88-3061T=
NM_001142649.2:c.136-210T= NP_001136121.1:n.136-210T=
NM_213599.3:c.139-210T= MANE Select NP_998764.1:n.139-210T=