Canonical Allele Identifier: CA379923976
Gene: ANO5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22272948G>C , CM000673.2:g.22272948G>C GRCh38
NC_000011.9:g.22294494G>C , CM000673.1:g.22294494G>C GRCh37
NC_000011.8:g.22251070G>C NCBI36
NG_015844.1:g.84773G>C , LRG_868:g.84773G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.211G>C
ENST00000682266.1:c.1744G>C ENSP00000507766.1:p.Asp582His
ENST00000682341.1:c.2152G>C ENSP00000508251.1:p.Asp718His
ENST00000683197.1:c.2152G>C ENSP00000507641.1:p.Asp718His
ENST00000683411.1:c.1744G>C ENSP00000508397.1:p.Asp582His
ENST00000683437.1:c.1744G>C ENSP00000508408.1:p.Asp582His
ENST00000683613.1:n.3188G>C
ENST00000684663.1:c.2149G>C ENSP00000508009.1:p.Asp717His
ENST00000324559.9:c.2194G>C MANE Select ENSP00000315371.9:p.Asp732His
ENST00000648804.1:n.2529G>C
ENST00000324559.8:c.2194G>C ENSP00000315371.8:p.Asp732His
ENST00000532043.1:n.211G>C
NM_001142649.1:c.2191G>C NP_001136121.1:p.Asp731His
NM_213599.2:c.2194G>C , LRG_868t1:c.2194G>C NP_998764.1:p.Asp732His
XM_005252820.2:c.2152G>C XP_005252877.2:p.Asp718His
XM_005252821.2:c.2149G>C XP_005252878.2:p.Asp717His
XM_005252822.3:c.2116G>C XP_005252879.1:p.Asp706His
XM_005252823.3:c.2113G>C XP_005252880.1:p.Asp705His
XM_011519949.1:c.2101G>C XP_011518251.1:p.Asp701His
XM_005252820.3:c.2152G>C XP_005252877.2:p.Asp718His
XM_005252821.3:c.2149G>C XP_005252878.2:p.Asp717His
XM_005252822.4:c.2116G>C XP_005252879.1:p.Asp706His
XM_011519949.2:c.2101G>C XP_011518251.1:p.Asp701His
NM_001142649.2:c.2191G>C NP_001136121.1:p.Asp731His
NM_213599.3:c.2194G>C MANE Select NP_998764.1:p.Asp732His