Canonical Allele Identifier: CA2574781456
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22250363_22250375del , CM000673.2:g.22250363_22250375del GRCh38
NC_000011.9:g.22271909_22271921del , CM000673.1:g.22271909_22271921del GRCh37
NC_000011.8:g.22228485_22228497del NCBI36
NG_015844.1:g.62188_62200del , LRG_868:g.62188_62200del

Transcript Alleles

HGVS Amino-acid change
ENST00000682089.1:n.325_333+4del
ENST00000682266.1:c.555_563+4del
ENST00000682341.1:c.963_971+4del
ENST00000682530.1:c.*937_*945+4del
ENST00000683197.1:c.963_971+4del
ENST00000683411.1:c.555_563+4del
ENST00000683437.1:c.555_563+4del
ENST00000683613.1:n.1999_2007+4del
ENST00000683834.1:n.1205_1213+4del
ENST00000684663.1:c.960_968+4del
ENST00000324559.9:c.1005_1013+4del
ENST00000648804.1:n.1340_1348+4del
ENST00000324559.8:c.1005_1013+4del
NM_001142649.1:c.1002_1010+4del
NM_213599.2:c.1005_1013+4del , LRG_868t1:c.1005_1013+4del
XM_005252820.2:c.963_971+4del
XM_005252821.2:c.960_968+4del
XM_005252822.3:c.927_935+4del
XM_005252823.3:c.924_932+4del
XM_011519949.1:c.912_920+4del
XM_005252820.3:c.963_971+4del
XM_005252821.3:c.960_968+4del
XM_005252822.4:c.927_935+4del
XM_011519949.2:c.912_920+4del
NM_001142649.2:c.1002_1010+4del
NM_213599.3:c.1005_1013+4del