Canonical Allele Identifier: CA2612864543

Gene: ANO5

Linked Data

• gnomAD v4: 11-22218145-A-ACACACACACACACAC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218145_22218146insCACACACACACACAC , CM000673.2:g.22218145_22218146insCACACACACACACAC	GRCh38
NC_000011.9:g.22239691_22239692insCACACACACACACAC , CM000673.1:g.22239691_22239692insCACACACACACACAC	GRCh37
NC_000011.8:g.22196267_22196268insCACACACACACACAC	NCBI36
NG_015844.1:g.29970_29971insCACACACACACACAC , LRG_868:g.29970_29971insCACACACACACACAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000682084.1:n.3313-101_3313-100insCACACACACACACAC
ENST00000682266.1:c.-270-2952_-270-2951insCACACACACACACAC	ENSP00000507766.1:n.-270-2952_-270-2951insCACACACACACACAC
ENST00000682341.1:c.139-2952_139-2951insCACACACACACACAC	ENSP00000508251.1:n.139-2952_139-2951insCACACACACACACAC
ENST00000682530.1:c.136-598_136-597insCACACACACACACAC	ENSP00000506805.1:n.136-598_136-597insCACACACACACACAC
ENST00000682684.1:n.560-2952_560-2951insCACACACACACACAC
ENST00000683197.1:c.139-2952_139-2951insCACACACACACACAC	ENSP00000507641.1:n.139-2952_139-2951insCACACACACACACAC
ENST00000683411.1:c.-270-2952_-270-2951insCACACACACACACAC	ENSP00000508397.1:n.-270-2952_-270-2951insCACACACACACACAC
ENST00000683437.1:c.-270-2952_-270-2951insCACACACACACACAC	ENSP00000508408.1:n.-270-2952_-270-2951insCACACACACACACAC
ENST00000683834.1:n.381-2952_381-2951insCACACACACACACAC
ENST00000683897.1:n.425-2952_425-2951insCACACACACACACAC
ENST00000684365.1:n.550-2952_550-2951insCACACACACACACAC
ENST00000684663.1:c.136-2952_136-2951insCACACACACACACAC	ENSP00000508009.1:n.136-2952_136-2951insCACACACACACACAC
ENST00000324559.9:c.139-101_139-100insCACACACACACACAC MANE Select	ENSP00000315371.9:n.139-101_139-100insCACACACACACACAC
ENST00000648804.1:n.670-441_670-440insCACACACACACACAC
ENST00000324559.8:c.139-101_139-100insCACACACACACACAC	ENSP00000315371.8:n.139-101_139-100insCACACACACACACAC
NM_001142649.1:c.136-101_136-100insCACACACACACACAC	NP_001136121.1:n.136-101_136-100insCACACACACACACAC
NM_213599.2:c.139-101_139-100insCACACACACACACAC , LRG_868t1:c.139-101_139-100insCACACACACACACAC	NP_998764.1:n.139-101_139-100insCACACACACACACAC
XM_005252820.2:c.139-2952_139-2951insCACACACACACACAC	XP_005252877.2:n.139-2952_139-2951insCACACACACACACAC
XM_005252821.2:c.136-2952_136-2951insCACACACACACACAC	XP_005252878.2:n.136-2952_136-2951insCACACACACACACAC
XM_005252822.3:c.61-101_61-100insCACACACACACACAC	XP_005252879.1:n.61-101_61-100insCACACACACACACAC
XM_005252823.3:c.58-101_58-100insCACACACACACACAC	XP_005252880.1:n.58-101_58-100insCACACACACACACAC
XM_011519949.1:c.88-2952_88-2951insCACACACACACACAC	XP_011518251.1:n.88-2952_88-2951insCACACACACACACAC
XM_005252820.3:c.139-2952_139-2951insCACACACACACACAC	XP_005252877.2:n.139-2952_139-2951insCACACACACACACAC
XM_005252821.3:c.136-2952_136-2951insCACACACACACACAC	XP_005252878.2:n.136-2952_136-2951insCACACACACACACAC
XM_005252822.4:c.61-101_61-100insCACACACACACACAC	XP_005252879.1:n.61-101_61-100insCACACACACACACAC
XM_011519949.2:c.88-2952_88-2951insCACACACACACACAC	XP_011518251.1:n.88-2952_88-2951insCACACACACACACAC
NM_001142649.2:c.136-101_136-100insCACACACACACACAC	NP_001136121.1:n.136-101_136-100insCACACACACACACAC
NM_213599.3:c.139-101_139-100insCACACACACACACAC MANE Select	NP_998764.1:n.139-101_139-100insCACACACACACACAC