Canonical Allele Identifier: CA1957416884

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255330_22255343delinsCTTTTTTAATATCT , CM000673.2:g.22255330_22255343delinsCTTTTTTAATATCT	GRCh38
NC_000011.9:g.22276876_22276889delinsCTTTTTTAATATCT , CM000673.1:g.22276876_22276889delinsCTTTTTTAATATCT	GRCh37
NC_000011.8:g.22233452_22233465delinsCTTTTTTAATATCT	NCBI36
NG_015844.1:g.67155_67168delinsCTTTTTTAATATCT , LRG_868:g.67155_67168delinsCTTTTTTAATATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.501-41_501-28delinsCTTTTTTAATATCT
ENST00000682266.1:c.731-41_731-28delinsCTTTTTTAATATCT	ENSP00000507766.1:n.731-41_731-28delinsCTTTTTTAATATCT
ENST00000682341.1:c.1139-41_1139-28delinsCTTTTTTAATATCT	ENSP00000508251.1:n.1139-41_1139-28delinsCTTTTTTAATATCT
ENST00000682530.1:c.*1113-41_*1113-28delinsCTTTTTTAATATCT	ENSP00000506805.1:n.*1113-41_*1113-28delinsCTTTTTTAATATCT
ENST00000683197.1:c.1139-41_1139-28delinsCTTTTTTAATATCT	ENSP00000507641.1:n.1139-41_1139-28delinsCTTTTTTAATATCT
ENST00000683411.1:c.731-41_731-28delinsCTTTTTTAATATCT	ENSP00000508397.1:n.731-41_731-28delinsCTTTTTTAATATCT
ENST00000683437.1:c.731-41_731-28delinsCTTTTTTAATATCT	ENSP00000508408.1:n.731-41_731-28delinsCTTTTTTAATATCT
ENST00000683613.1:n.2175-41_2175-28delinsCTTTTTTAATATCT
ENST00000683834.1:n.1381-41_1381-28delinsCTTTTTTAATATCT
ENST00000684663.1:c.1136-41_1136-28delinsCTTTTTTAATATCT	ENSP00000508009.1:n.1136-41_1136-28delinsCTTTTTTAATATCT
ENST00000324559.9:c.1181-41_1181-28delinsCTTTTTTAATATCT MANE Select	ENSP00000315371.9:n.1181-41_1181-28delinsCTTTTTTAATATCT
ENST00000648804.1:n.1516-41_1516-28delinsCTTTTTTAATATCT
ENST00000324559.8:c.1181-41_1181-28delinsCTTTTTTAATATCT	ENSP00000315371.8:n.1181-41_1181-28delinsCTTTTTTAATATCT
NM_001142649.1:c.1178-41_1178-28delinsCTTTTTTAATATCT	NP_001136121.1:n.1178-41_1178-28delinsCTTTTTTAATATCT
NM_213599.2:c.1181-41_1181-28delinsCTTTTTTAATATCT , LRG_868t1:c.1181-41_1181-28delinsCTTTTTTAATATCT	NP_998764.1:n.1181-41_1181-28delinsCTTTTTTAATATCT
XM_005252820.2:c.1139-41_1139-28delinsCTTTTTTAATATCT	XP_005252877.2:n.1139-41_1139-28delinsCTTTTTTAATATCT
XM_005252821.2:c.1136-41_1136-28delinsCTTTTTTAATATCT	XP_005252878.2:n.1136-41_1136-28delinsCTTTTTTAATATCT
XM_005252822.3:c.1103-41_1103-28delinsCTTTTTTAATATCT	XP_005252879.1:n.1103-41_1103-28delinsCTTTTTTAATATCT
XM_005252823.3:c.1100-41_1100-28delinsCTTTTTTAATATCT	XP_005252880.1:n.1100-41_1100-28delinsCTTTTTTAATATCT
XM_011519949.1:c.1088-41_1088-28delinsCTTTTTTAATATCT	XP_011518251.1:n.1088-41_1088-28delinsCTTTTTTAATATCT
XM_005252820.3:c.1139-41_1139-28delinsCTTTTTTAATATCT	XP_005252877.2:n.1139-41_1139-28delinsCTTTTTTAATATCT
XM_005252821.3:c.1136-41_1136-28delinsCTTTTTTAATATCT	XP_005252878.2:n.1136-41_1136-28delinsCTTTTTTAATATCT
XM_005252822.4:c.1103-41_1103-28delinsCTTTTTTAATATCT	XP_005252879.1:n.1103-41_1103-28delinsCTTTTTTAATATCT
XM_011519949.2:c.1088-41_1088-28delinsCTTTTTTAATATCT	XP_011518251.1:n.1088-41_1088-28delinsCTTTTTTAATATCT
NM_001142649.2:c.1178-41_1178-28delinsCTTTTTTAATATCT	NP_001136121.1:n.1178-41_1178-28delinsCTTTTTTAATATCT
NM_213599.3:c.1181-41_1181-28delinsCTTTTTTAATATCT MANE Select	NP_998764.1:n.1181-41_1181-28delinsCTTTTTTAATATCT