Canonical Allele Identifier: CA2612864308

Gene: ANO5

Linked Data

• gnomAD v4: 11-22218117-A-ACACACACACACACACG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218132_22218133insGCACACACACACACAC , CM000673.2:g.22218132_22218133insGCACACACACACACAC	GRCh38
NC_000011.9:g.22239678_22239679insGCACACACACACACAC , CM000673.1:g.22239678_22239679insGCACACACACACACAC	GRCh37
NC_000011.8:g.22196254_22196255insGCACACACACACACAC	NCBI36
NG_015844.1:g.29957_29958insGCACACACACACACAC , LRG_868:g.29957_29958insGCACACACACACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682084.1:n.3313-114_3313-113insGCACACACACACACAC
ENST00000682266.1:c.-270-2965_-270-2964insGCACACACACACACAC	ENSP00000507766.1:n.-270-2965_-270-2964insGCACACACACACACAC
ENST00000682341.1:c.139-2965_139-2964insGCACACACACACACAC	ENSP00000508251.1:n.139-2965_139-2964insGCACACACACACACAC
ENST00000682530.1:c.136-611_136-610insGCACACACACACACAC	ENSP00000506805.1:n.136-611_136-610insGCACACACACACACAC
ENST00000682684.1:n.560-2965_560-2964insGCACACACACACACAC
ENST00000683197.1:c.139-2965_139-2964insGCACACACACACACAC	ENSP00000507641.1:n.139-2965_139-2964insGCACACACACACACAC
ENST00000683411.1:c.-270-2965_-270-2964insGCACACACACACACAC	ENSP00000508397.1:n.-270-2965_-270-2964insGCACACACACACACAC
ENST00000683437.1:c.-270-2965_-270-2964insGCACACACACACACAC	ENSP00000508408.1:n.-270-2965_-270-2964insGCACACACACACACAC
ENST00000683834.1:n.381-2965_381-2964insGCACACACACACACAC
ENST00000683897.1:n.425-2965_425-2964insGCACACACACACACAC
ENST00000684365.1:n.550-2965_550-2964insGCACACACACACACAC
ENST00000684663.1:c.136-2965_136-2964insGCACACACACACACAC	ENSP00000508009.1:n.136-2965_136-2964insGCACACACACACACAC
ENST00000324559.9:c.139-114_139-113insGCACACACACACACAC MANE Select	ENSP00000315371.9:n.139-114_139-113insGCACACACACACACAC
ENST00000648804.1:n.670-454_670-453insGCACACACACACACAC
ENST00000324559.8:c.139-114_139-113insGCACACACACACACAC	ENSP00000315371.8:n.139-114_139-113insGCACACACACACACAC
NM_001142649.1:c.136-114_136-113insGCACACACACACACAC	NP_001136121.1:n.136-114_136-113insGCACACACACACACAC
NM_213599.2:c.139-114_139-113insGCACACACACACACAC , LRG_868t1:c.139-114_139-113insGCACACACACACACAC	NP_998764.1:n.139-114_139-113insGCACACACACACACAC
XM_005252820.2:c.139-2965_139-2964insGCACACACACACACAC	XP_005252877.2:n.139-2965_139-2964insGCACACACACACACAC
XM_005252821.2:c.136-2965_136-2964insGCACACACACACACAC	XP_005252878.2:n.136-2965_136-2964insGCACACACACACACAC
XM_005252822.3:c.61-114_61-113insGCACACACACACACAC	XP_005252879.1:n.61-114_61-113insGCACACACACACACAC
XM_005252823.3:c.58-114_58-113insGCACACACACACACAC	XP_005252880.1:n.58-114_58-113insGCACACACACACACAC
XM_011519949.1:c.88-2965_88-2964insGCACACACACACACAC	XP_011518251.1:n.88-2965_88-2964insGCACACACACACACAC
XM_005252820.3:c.139-2965_139-2964insGCACACACACACACAC	XP_005252877.2:n.139-2965_139-2964insGCACACACACACACAC
XM_005252821.3:c.136-2965_136-2964insGCACACACACACACAC	XP_005252878.2:n.136-2965_136-2964insGCACACACACACACAC
XM_005252822.4:c.61-114_61-113insGCACACACACACACAC	XP_005252879.1:n.61-114_61-113insGCACACACACACACAC
XM_011519949.2:c.88-2965_88-2964insGCACACACACACACAC	XP_011518251.1:n.88-2965_88-2964insGCACACACACACACAC
NM_001142649.2:c.136-114_136-113insGCACACACACACACAC	NP_001136121.1:n.136-114_136-113insGCACACACACACACAC
NM_213599.3:c.139-114_139-113insGCACACACACACACAC MANE Select	NP_998764.1:n.139-114_139-113insGCACACACACACACAC