Canonical Allele Identifier: CA2612864706

Gene: ANO5

Linked Data

• gnomAD v4: 11-22221006-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22221009del , CM000673.2:g.22221009del	GRCh38
NC_000011.9:g.22242555del , CM000673.1:g.22242555del	GRCh37
NC_000011.8:g.22199131del	NCBI36
NG_015844.1:g.32834del , LRG_868:g.32834del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.-270-88del	ENSP00000507766.1:n.-270-88del
ENST00000682341.1:c.139-88del	ENSP00000508251.1:n.139-88del
ENST00000682530.1:c.*113-88del	ENSP00000506805.1:n.*113-88del
ENST00000682684.1:n.560-88del
ENST00000683197.1:c.139-88del	ENSP00000507641.1:n.139-88del
ENST00000683411.1:c.-270-88del	ENSP00000508397.1:n.-270-88del
ENST00000683437.1:c.-270-88del	ENSP00000508408.1:n.-270-88del
ENST00000683613.1:n.1087del
ENST00000683834.1:n.381-88del
ENST00000683897.1:n.425-88del
ENST00000684365.1:n.550-88del
ENST00000684663.1:c.136-88del	ENSP00000508009.1:n.136-88del
ENST00000324559.9:c.181-88del MANE Select	ENSP00000315371.9:n.181-88del
ENST00000648804.1:n.746-88del
ENST00000324559.8:c.181-88del	ENSP00000315371.8:n.181-88del
NM_001142649.1:c.178-88del	NP_001136121.1:n.178-88del
NM_213599.2:c.181-88del , LRG_868t1:c.181-88del	NP_998764.1:n.181-88del
XM_005252820.2:c.139-88del	XP_005252877.2:n.139-88del
XM_005252821.2:c.136-88del	XP_005252878.2:n.136-88del
XM_005252822.3:c.103-88del	XP_005252879.1:n.103-88del
XM_005252823.3:c.100-88del	XP_005252880.1:n.100-88del
XM_011519949.1:c.88-88del	XP_011518251.1:n.88-88del
XM_005252820.3:c.139-88del	XP_005252877.2:n.139-88del
XM_005252821.3:c.136-88del	XP_005252878.2:n.136-88del
XM_005252822.4:c.103-88del	XP_005252879.1:n.103-88del
XM_011519949.2:c.88-88del	XP_011518251.1:n.88-88del
NM_001142649.2:c.178-88del	NP_001136121.1:n.178-88del
NM_213599.3:c.181-88del MANE Select	NP_998764.1:n.181-88del