Canonical Allele Identifier: CA1957416877

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255321_22255322delinsAG , CM000673.2:g.22255321_22255322delinsAG	GRCh38
NC_000011.9:g.22276867_22276868delinsAG , CM000673.1:g.22276867_22276868delinsAG	GRCh37
NC_000011.8:g.22233443_22233444delinsAG	NCBI36
NG_015844.1:g.67146_67147delinsAG , LRG_868:g.67146_67147delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.501-50_501-49delinsAG
ENST00000682266.1:c.731-50_731-49delinsAG	ENSP00000507766.1:n.731-50_731-49delinsAG
ENST00000682341.1:c.1139-50_1139-49delinsAG	ENSP00000508251.1:n.1139-50_1139-49delinsAG
ENST00000682530.1:c.*1113-50_*1113-49delinsAG	ENSP00000506805.1:n.*1113-50_*1113-49delinsAG
ENST00000683197.1:c.1139-50_1139-49delinsAG	ENSP00000507641.1:n.1139-50_1139-49delinsAG
ENST00000683411.1:c.731-50_731-49delinsAG	ENSP00000508397.1:n.731-50_731-49delinsAG
ENST00000683437.1:c.731-50_731-49delinsAG	ENSP00000508408.1:n.731-50_731-49delinsAG
ENST00000683613.1:n.2175-50_2175-49delinsAG
ENST00000683834.1:n.1381-50_1381-49delinsAG
ENST00000684663.1:c.1136-50_1136-49delinsAG	ENSP00000508009.1:n.1136-50_1136-49delinsAG
ENST00000324559.9:c.1181-50_1181-49delinsAG MANE Select	ENSP00000315371.9:n.1181-50_1181-49delinsAG
ENST00000648804.1:n.1516-50_1516-49delinsAG
ENST00000324559.8:c.1181-50_1181-49delinsAG	ENSP00000315371.8:n.1181-50_1181-49delinsAG
NM_001142649.1:c.1178-50_1178-49delinsAG	NP_001136121.1:n.1178-50_1178-49delinsAG
NM_213599.2:c.1181-50_1181-49delinsAG , LRG_868t1:c.1181-50_1181-49delinsAG	NP_998764.1:n.1181-50_1181-49delinsAG
XM_005252820.2:c.1139-50_1139-49delinsAG	XP_005252877.2:n.1139-50_1139-49delinsAG
XM_005252821.2:c.1136-50_1136-49delinsAG	XP_005252878.2:n.1136-50_1136-49delinsAG
XM_005252822.3:c.1103-50_1103-49delinsAG	XP_005252879.1:n.1103-50_1103-49delinsAG
XM_005252823.3:c.1100-50_1100-49delinsAG	XP_005252880.1:n.1100-50_1100-49delinsAG
XM_011519949.1:c.1088-50_1088-49delinsAG	XP_011518251.1:n.1088-50_1088-49delinsAG
XM_005252820.3:c.1139-50_1139-49delinsAG	XP_005252877.2:n.1139-50_1139-49delinsAG
XM_005252821.3:c.1136-50_1136-49delinsAG	XP_005252878.2:n.1136-50_1136-49delinsAG
XM_005252822.4:c.1103-50_1103-49delinsAG	XP_005252879.1:n.1103-50_1103-49delinsAG
XM_011519949.2:c.1088-50_1088-49delinsAG	XP_011518251.1:n.1088-50_1088-49delinsAG
NM_001142649.2:c.1178-50_1178-49delinsAG	NP_001136121.1:n.1178-50_1178-49delinsAG
NM_213599.3:c.1181-50_1181-49delinsAG MANE Select	NP_998764.1:n.1181-50_1181-49delinsAG