Canonical Allele Identifier: CA1957393827
Gene: ANO5 HGNC NCBI

Linked Data

dbSNP Id: rs1852512515

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22218076_22218086del , CM000673.2:g.22218076_22218086del GRCh38
NC_000011.9:g.22239622_22239632del , CM000673.1:g.22239622_22239632del GRCh37
NC_000011.8:g.22196198_22196208del NCBI36
NG_015844.1:g.29901_29911del , LRG_868:g.29901_29911del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682084.1:n.3313-170_3313-160del
ENST00000682266.1:c.-270-3021_-270-3011del ENSP00000507766.1:n.-270-3021_-270-3011del
ENST00000682341.1:c.139-3021_139-3011del ENSP00000508251.1:n.139-3021_139-3011del
ENST00000682530.1:c.136-667_136-657del ENSP00000506805.1:n.136-667_136-657del
ENST00000682684.1:n.560-3021_560-3011del
ENST00000683197.1:c.139-3021_139-3011del ENSP00000507641.1:n.139-3021_139-3011del
ENST00000683411.1:c.-270-3021_-270-3011del ENSP00000508397.1:n.-270-3021_-270-3011del
ENST00000683437.1:c.-270-3021_-270-3011del ENSP00000508408.1:n.-270-3021_-270-3011del
ENST00000683834.1:n.381-3021_381-3011del
ENST00000683897.1:n.425-3021_425-3011del
ENST00000684365.1:n.550-3021_550-3011del
ENST00000684663.1:c.136-3021_136-3011del ENSP00000508009.1:n.136-3021_136-3011del
ENST00000324559.9:c.139-170_139-160del MANE Select ENSP00000315371.9:n.139-170_139-160del
ENST00000648804.1:n.670-510_670-500del
ENST00000324559.8:c.139-170_139-160del ENSP00000315371.8:n.139-170_139-160del
NM_001142649.1:c.136-170_136-160del NP_001136121.1:n.136-170_136-160del
NM_213599.2:c.139-170_139-160del , LRG_868t1:c.139-170_139-160del NP_998764.1:n.139-170_139-160del
XM_005252820.2:c.139-3021_139-3011del XP_005252877.2:n.139-3021_139-3011del
XM_005252821.2:c.136-3021_136-3011del XP_005252878.2:n.136-3021_136-3011del
XM_005252822.3:c.61-170_61-160del XP_005252879.1:n.61-170_61-160del
XM_005252823.3:c.58-170_58-160del XP_005252880.1:n.58-170_58-160del
XM_011519949.1:c.88-3021_88-3011del XP_011518251.1:n.88-3021_88-3011del
XM_005252820.3:c.139-3021_139-3011del XP_005252877.2:n.139-3021_139-3011del
XM_005252821.3:c.136-3021_136-3011del XP_005252878.2:n.136-3021_136-3011del
XM_005252822.4:c.61-170_61-160del XP_005252879.1:n.61-170_61-160del
XM_011519949.2:c.88-3021_88-3011del XP_011518251.1:n.88-3021_88-3011del
NM_001142649.2:c.136-170_136-160del NP_001136121.1:n.136-170_136-160del
NM_213599.3:c.139-170_139-160del MANE Select NP_998764.1:n.139-170_139-160del