Canonical Allele Identifier: CA1957397427
Gene: ANO5 HGNC NCBI

Linked Data

dbSNP Id: rs1852813682

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22225959T>C , CM000673.2:g.22225959T>C GRCh38
NC_000011.9:g.22247505T>C , CM000673.1:g.22247505T>C GRCh37
NC_000011.8:g.22204081T>C NCBI36
NG_015844.1:g.37784T>C , LRG_868:g.37784T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682266.1:c.-156-25T>C ENSP00000507766.1:n.-156-25T>C
ENST00000682341.1:c.253-25T>C ENSP00000508251.1:n.253-25T>C
ENST00000682530.1:c.*227-25T>C ENSP00000506805.1:n.*227-25T>C
ENST00000682684.1:n.674-25T>C
ENST00000683197.1:c.253-25T>C ENSP00000507641.1:n.253-25T>C
ENST00000683411.1:c.-156-25T>C ENSP00000508397.1:n.-156-25T>C
ENST00000683437.1:c.-156-25T>C ENSP00000508408.1:n.-156-25T>C
ENST00000683613.1:n.1289-25T>C
ENST00000683834.1:n.495-25T>C
ENST00000684663.1:c.250-25T>C ENSP00000508009.1:n.250-25T>C
ENST00000324559.9:c.295-25T>C MANE Select ENSP00000315371.9:n.295-25T>C
ENST00000648804.1:n.860-25T>C
ENST00000324559.8:c.295-25T>C ENSP00000315371.8:n.295-25T>C
NM_001142649.1:c.292-25T>C NP_001136121.1:n.292-25T>C
NM_213599.2:c.295-25T>C , LRG_868t1:c.295-25T>C NP_998764.1:n.295-25T>C
XM_005252820.2:c.253-25T>C XP_005252877.2:n.253-25T>C
XM_005252821.2:c.250-25T>C XP_005252878.2:n.250-25T>C
XM_005252822.3:c.217-25T>C XP_005252879.1:n.217-25T>C
XM_005252823.3:c.214-25T>C XP_005252880.1:n.214-25T>C
XM_011519949.1:c.202-25T>C XP_011518251.1:n.202-25T>C
XM_005252820.3:c.253-25T>C XP_005252877.2:n.253-25T>C
XM_005252821.3:c.250-25T>C XP_005252878.2:n.250-25T>C
XM_005252822.4:c.217-25T>C XP_005252879.1:n.217-25T>C
XM_011519949.2:c.202-25T>C XP_011518251.1:n.202-25T>C
NM_001142649.2:c.292-25T>C NP_001136121.1:n.292-25T>C
NM_213599.3:c.295-25T>C MANE Select NP_998764.1:n.295-25T>C