Canonical Allele Identifier: CA2612864915
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22225975_22225976dup , CM000673.2:g.22225975_22225976dup GRCh38
NC_000011.9:g.22247521_22247522dup , CM000673.1:g.22247521_22247522dup GRCh37
NC_000011.8:g.22204097_22204098dup NCBI36
NG_015844.1:g.37800_37801dup , LRG_868:g.37800_37801dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682266.1:c.-156-9_-156-8dup ENSP00000507766.1:n.-156-9_-156-8dup
ENST00000682341.1:c.253-9_253-8dup ENSP00000508251.1:n.253-9_253-8dup
ENST00000682530.1:c.*227-9_*227-8dup ENSP00000506805.1:n.*227-9_*227-8dup
ENST00000682684.1:n.674-9_674-8dup
ENST00000683197.1:c.253-9_253-8dup ENSP00000507641.1:n.253-9_253-8dup
ENST00000683411.1:c.-156-9_-156-8dup ENSP00000508397.1:n.-156-9_-156-8dup
ENST00000683437.1:c.-156-9_-156-8dup ENSP00000508408.1:n.-156-9_-156-8dup
ENST00000683613.1:n.1289-9_1289-8dup
ENST00000683834.1:n.495-9_495-8dup
ENST00000684663.1:c.250-9_250-8dup ENSP00000508009.1:n.250-9_250-8dup
ENST00000324559.9:c.295-9_295-8dup MANE Select ENSP00000315371.9:n.295-9_295-8dup
ENST00000648804.1:n.860-9_860-8dup
ENST00000324559.8:c.295-9_295-8dup ENSP00000315371.8:n.295-9_295-8dup
NM_001142649.1:c.292-9_292-8dup NP_001136121.1:n.292-9_292-8dup
NM_213599.2:c.295-9_295-8dup , LRG_868t1:c.295-9_295-8dup NP_998764.1:n.295-9_295-8dup
XM_005252820.2:c.253-9_253-8dup XP_005252877.2:n.253-9_253-8dup
XM_005252821.2:c.250-9_250-8dup XP_005252878.2:n.250-9_250-8dup
XM_005252822.3:c.217-9_217-8dup XP_005252879.1:n.217-9_217-8dup
XM_005252823.3:c.214-9_214-8dup XP_005252880.1:n.214-9_214-8dup
XM_011519949.1:c.202-9_202-8dup XP_011518251.1:n.202-9_202-8dup
XM_005252820.3:c.253-9_253-8dup XP_005252877.2:n.253-9_253-8dup
XM_005252821.3:c.250-9_250-8dup XP_005252878.2:n.250-9_250-8dup
XM_005252822.4:c.217-9_217-8dup XP_005252879.1:n.217-9_217-8dup
XM_011519949.2:c.202-9_202-8dup XP_011518251.1:n.202-9_202-8dup
NM_001142649.2:c.292-9_292-8dup NP_001136121.1:n.292-9_292-8dup
NM_213599.3:c.295-9_295-8dup MANE Select NP_998764.1:n.295-9_295-8dup