Canonical Allele Identifier: CA379920680
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22250257T>G , CM000673.2:g.22250257T>G GRCh38
NC_000011.9:g.22271803T>G , CM000673.1:g.22271803T>G GRCh37
NC_000011.8:g.22228379T>G NCBI36
NG_015844.1:g.62082T>G , LRG_868:g.62082T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682089.1:n.219T>G
ENST00000682266.1:c.449T>G ENSP00000507766.1:p.Ile150Ser
ENST00000682341.1:c.857T>G ENSP00000508251.1:p.Ile286Ser
ENST00000682530.1:c.*831T>G ENSP00000506805.1:n.*831T>G
ENST00000683197.1:c.857T>G ENSP00000507641.1:p.Ile286Ser
ENST00000683411.1:c.449T>G ENSP00000508397.1:p.Ile150Ser
ENST00000683437.1:c.449T>G ENSP00000508408.1:p.Ile150Ser
ENST00000683613.1:n.1893T>G
ENST00000683834.1:n.1099T>G
ENST00000684663.1:c.854T>G ENSP00000508009.1:p.Ile285Ser
ENST00000324559.9:c.899T>G MANE Select ENSP00000315371.9:p.Ile300Ser
ENST00000648804.1:n.1234T>G
ENST00000324559.8:c.899T>G ENSP00000315371.8:p.Ile300Ser
NM_001142649.1:c.896T>G NP_001136121.1:p.Ile299Ser
NM_213599.2:c.899T>G , LRG_868t1:c.899T>G NP_998764.1:p.Ile300Ser
XM_005252820.2:c.857T>G XP_005252877.2:p.Ile286Ser
XM_005252821.2:c.854T>G XP_005252878.2:p.Ile285Ser
XM_005252822.3:c.821T>G XP_005252879.1:p.Ile274Ser
XM_005252823.3:c.818T>G XP_005252880.1:p.Ile273Ser
XM_011519949.1:c.806T>G XP_011518251.1:p.Ile269Ser
XM_005252820.3:c.857T>G XP_005252877.2:p.Ile286Ser
XM_005252821.3:c.854T>G XP_005252878.2:p.Ile285Ser
XM_005252822.4:c.821T>G XP_005252879.1:p.Ile274Ser
XM_011519949.2:c.806T>G XP_011518251.1:p.Ile269Ser
NM_001142649.2:c.896T>G NP_001136121.1:p.Ile299Ser
NM_213599.3:c.899T>G MANE Select NP_998764.1:p.Ile300Ser