Canonical Allele Identifier: CA2612864548

Gene: ANO5

Linked Data

• gnomAD v4: 11-22218146-A-ACACACACACACACACAC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218146_22218147insCACACACACACACACAC , CM000673.2:g.22218146_22218147insCACACACACACACACAC	GRCh38
NC_000011.9:g.22239692_22239693insCACACACACACACACAC , CM000673.1:g.22239692_22239693insCACACACACACACACAC	GRCh37
NC_000011.8:g.22196268_22196269insCACACACACACACACAC	NCBI36
NG_015844.1:g.29971_29972insCACACACACACACACAC , LRG_868:g.29971_29972insCACACACACACACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682084.1:n.3313-100_3313-99insCACACACACACACACAC
ENST00000682266.1:c.-270-2951_-270-2950insCACACACACACACACAC	ENSP00000507766.1:n.-270-2951_-270-2950insCACACACACACACACAC
ENST00000682341.1:c.139-2951_139-2950insCACACACACACACACAC	ENSP00000508251.1:n.139-2951_139-2950insCACACACACACACACAC
ENST00000682530.1:c.136-597_136-596insCACACACACACACACAC	ENSP00000506805.1:n.136-597_136-596insCACACACACACACACAC
ENST00000682684.1:n.560-2951_560-2950insCACACACACACACACAC
ENST00000683197.1:c.139-2951_139-2950insCACACACACACACACAC	ENSP00000507641.1:n.139-2951_139-2950insCACACACACACACACAC
ENST00000683411.1:c.-270-2951_-270-2950insCACACACACACACACAC	ENSP00000508397.1:n.-270-2951_-270-2950insCACACACACACACACAC
ENST00000683437.1:c.-270-2951_-270-2950insCACACACACACACACAC	ENSP00000508408.1:n.-270-2951_-270-2950insCACACACACACACACAC
ENST00000683834.1:n.381-2951_381-2950insCACACACACACACACAC
ENST00000683897.1:n.425-2951_425-2950insCACACACACACACACAC
ENST00000684365.1:n.550-2951_550-2950insCACACACACACACACAC
ENST00000684663.1:c.136-2951_136-2950insCACACACACACACACAC	ENSP00000508009.1:n.136-2951_136-2950insCACACACACACACACAC
ENST00000324559.9:c.139-100_139-99insCACACACACACACACAC MANE Select	ENSP00000315371.9:n.139-100_139-99insCACACACACACACACAC
ENST00000648804.1:n.670-440_670-439insCACACACACACACACAC
ENST00000324559.8:c.139-100_139-99insCACACACACACACACAC	ENSP00000315371.8:n.139-100_139-99insCACACACACACACACAC
NM_001142649.1:c.136-100_136-99insCACACACACACACACAC	NP_001136121.1:n.136-100_136-99insCACACACACACACACAC
NM_213599.2:c.139-100_139-99insCACACACACACACACAC , LRG_868t1:c.139-100_139-99insCACACACACACACACAC	NP_998764.1:n.139-100_139-99insCACACACACACACACAC
XM_005252820.2:c.139-2951_139-2950insCACACACACACACACAC	XP_005252877.2:n.139-2951_139-2950insCACACACACACACACAC
XM_005252821.2:c.136-2951_136-2950insCACACACACACACACAC	XP_005252878.2:n.136-2951_136-2950insCACACACACACACACAC
XM_005252822.3:c.61-100_61-99insCACACACACACACACAC	XP_005252879.1:n.61-100_61-99insCACACACACACACACAC
XM_005252823.3:c.58-100_58-99insCACACACACACACACAC	XP_005252880.1:n.58-100_58-99insCACACACACACACACAC
XM_011519949.1:c.88-2951_88-2950insCACACACACACACACAC	XP_011518251.1:n.88-2951_88-2950insCACACACACACACACAC
XM_005252820.3:c.139-2951_139-2950insCACACACACACACACAC	XP_005252877.2:n.139-2951_139-2950insCACACACACACACACAC
XM_005252821.3:c.136-2951_136-2950insCACACACACACACACAC	XP_005252878.2:n.136-2951_136-2950insCACACACACACACACAC
XM_005252822.4:c.61-100_61-99insCACACACACACACACAC	XP_005252879.1:n.61-100_61-99insCACACACACACACACAC
XM_011519949.2:c.88-2951_88-2950insCACACACACACACACAC	XP_011518251.1:n.88-2951_88-2950insCACACACACACACACAC
NM_001142649.2:c.136-100_136-99insCACACACACACACACAC	NP_001136121.1:n.136-100_136-99insCACACACACACACACAC
NM_213599.3:c.139-100_139-99insCACACACACACACACAC MANE Select	NP_998764.1:n.139-100_139-99insCACACACACACACACAC