Canonical Allele Identifier: CA379923967
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22272944G>T , CM000673.2:g.22272944G>T GRCh38
NC_000011.9:g.22294490G>T , CM000673.1:g.22294490G>T GRCh37
NC_000011.8:g.22251066G>T NCBI36
NG_015844.1:g.84769G>T , LRG_868:g.84769G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.207G>T
ENST00000682266.1:c.1740G>T ENSP00000507766.1:p.Trp580Cys
ENST00000682341.1:c.2148G>T ENSP00000508251.1:p.Trp716Cys
ENST00000683197.1:c.2148G>T ENSP00000507641.1:p.Trp716Cys
ENST00000683411.1:c.1740G>T ENSP00000508397.1:p.Trp580Cys
ENST00000683437.1:c.1740G>T ENSP00000508408.1:p.Trp580Cys
ENST00000683613.1:n.3184G>T
ENST00000684663.1:c.2145G>T ENSP00000508009.1:p.Trp715Cys
ENST00000324559.9:c.2190G>T MANE Select ENSP00000315371.9:p.Trp730Cys
ENST00000648804.1:n.2525G>T
ENST00000324559.8:c.2190G>T ENSP00000315371.8:p.Trp730Cys
ENST00000532043.1:n.207G>T
NM_001142649.1:c.2187G>T NP_001136121.1:p.Trp729Cys
NM_213599.2:c.2190G>T , LRG_868t1:c.2190G>T NP_998764.1:p.Trp730Cys
XM_005252820.2:c.2148G>T XP_005252877.2:p.Trp716Cys
XM_005252821.2:c.2145G>T XP_005252878.2:p.Trp715Cys
XM_005252822.3:c.2112G>T XP_005252879.1:p.Trp704Cys
XM_005252823.3:c.2109G>T XP_005252880.1:p.Trp703Cys
XM_011519949.1:c.2097G>T XP_011518251.1:p.Trp699Cys
XM_005252820.3:c.2148G>T XP_005252877.2:p.Trp716Cys
XM_005252821.3:c.2145G>T XP_005252878.2:p.Trp715Cys
XM_005252822.4:c.2112G>T XP_005252879.1:p.Trp704Cys
XM_011519949.2:c.2097G>T XP_011518251.1:p.Trp699Cys
NM_001142649.2:c.2187G>T NP_001136121.1:p.Trp729Cys
NM_213599.3:c.2190G>T MANE Select NP_998764.1:p.Trp730Cys