Canonical Allele Identifier: CA5923166

Gene: ANO5

Linked Data

• dbSNP Id: rs752025573
• ExAC: 11:22276867 AG / A
• gnomAD v2: 11-22276867-AG-A
• gnomAD v4: 11-22255321-AG-A
• MyVariant Identifiers: chr11:g.22276868del (hg19) ; chr11:g.22255322del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255322del , CM000673.2:g.22255322del	GRCh38
NC_000011.9:g.22276868del , CM000673.1:g.22276868del	GRCh37
NC_000011.8:g.22233444del	NCBI36
NG_015844.1:g.67147del , LRG_868:g.67147del

Transcript Alleles

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