Canonical Allele Identifier: CA379921626
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22255493A>C , CM000673.2:g.22255493A>C GRCh38
NC_000011.9:g.22277039A>C , CM000673.1:g.22277039A>C GRCh37
NC_000011.8:g.22233615A>C NCBI36
NG_015844.1:g.67318A>C , LRG_868:g.67318A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682089.1:n.623A>C
ENST00000682266.1:c.853A>C ENSP00000507766.1:p.Lys285Gln
ENST00000682341.1:c.1261A>C ENSP00000508251.1:p.Lys421Gln
ENST00000682530.1:c.*1235A>C ENSP00000506805.1:n.*1235A>C
ENST00000683197.1:c.1261A>C ENSP00000507641.1:p.Lys421Gln
ENST00000683411.1:c.853A>C ENSP00000508397.1:p.Lys285Gln
ENST00000683437.1:c.853A>C ENSP00000508408.1:p.Lys285Gln
ENST00000683613.1:n.2297A>C
ENST00000683834.1:n.1503A>C
ENST00000684663.1:c.1258A>C ENSP00000508009.1:p.Lys420Gln
ENST00000324559.9:c.1303A>C MANE Select ENSP00000315371.9:p.Lys435Gln
ENST00000648804.1:n.1638A>C
ENST00000324559.8:c.1303A>C ENSP00000315371.8:p.Lys435Gln
NM_001142649.1:c.1300A>C NP_001136121.1:p.Lys434Gln
NM_213599.2:c.1303A>C , LRG_868t1:c.1303A>C NP_998764.1:p.Lys435Gln
XM_005252820.2:c.1261A>C XP_005252877.2:p.Lys421Gln
XM_005252821.2:c.1258A>C XP_005252878.2:p.Lys420Gln
XM_005252822.3:c.1225A>C XP_005252879.1:p.Lys409Gln
XM_005252823.3:c.1222A>C XP_005252880.1:p.Lys408Gln
XM_011519949.1:c.1210A>C XP_011518251.1:p.Lys404Gln
XM_005252820.3:c.1261A>C XP_005252877.2:p.Lys421Gln
XM_005252821.3:c.1258A>C XP_005252878.2:p.Lys420Gln
XM_005252822.4:c.1225A>C XP_005252879.1:p.Lys409Gln
XM_011519949.2:c.1210A>C XP_011518251.1:p.Lys404Gln
NM_001142649.2:c.1300A>C NP_001136121.1:p.Lys434Gln
NM_213599.3:c.1303A>C MANE Select NP_998764.1:p.Lys435Gln