Canonical Allele Identifier: CA2612864537

Gene: ANO5

Linked Data

• gnomAD v4: 11-22218144-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218147_22218148del , CM000673.2:g.22218147_22218148del	GRCh38
NC_000011.9:g.22239693_22239694del , CM000673.1:g.22239693_22239694del	GRCh37
NC_000011.8:g.22196269_22196270del	NCBI36
NG_015844.1:g.29972_29973del , LRG_868:g.29972_29973del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682084.1:n.3313-99_3313-98del
ENST00000682266.1:c.-270-2950_-270-2949del	ENSP00000507766.1:n.-270-2950_-270-2949del
ENST00000682341.1:c.139-2950_139-2949del	ENSP00000508251.1:n.139-2950_139-2949del
ENST00000682530.1:c.136-596_136-595del	ENSP00000506805.1:n.136-596_136-595del
ENST00000682684.1:n.560-2950_560-2949del
ENST00000683197.1:c.139-2950_139-2949del	ENSP00000507641.1:n.139-2950_139-2949del
ENST00000683411.1:c.-270-2950_-270-2949del	ENSP00000508397.1:n.-270-2950_-270-2949del
ENST00000683437.1:c.-270-2950_-270-2949del	ENSP00000508408.1:n.-270-2950_-270-2949del
ENST00000683834.1:n.381-2950_381-2949del
ENST00000683897.1:n.425-2950_425-2949del
ENST00000684365.1:n.550-2950_550-2949del
ENST00000684663.1:c.136-2950_136-2949del	ENSP00000508009.1:n.136-2950_136-2949del
ENST00000324559.9:c.139-99_139-98del MANE Select	ENSP00000315371.9:n.139-99_139-98del
ENST00000648804.1:n.670-439_670-438del
ENST00000324559.8:c.139-99_139-98del	ENSP00000315371.8:n.139-99_139-98del
NM_001142649.1:c.136-99_136-98del	NP_001136121.1:n.136-99_136-98del
NM_213599.2:c.139-99_139-98del , LRG_868t1:c.139-99_139-98del	NP_998764.1:n.139-99_139-98del
XM_005252820.2:c.139-2950_139-2949del	XP_005252877.2:n.139-2950_139-2949del
XM_005252821.2:c.136-2950_136-2949del	XP_005252878.2:n.136-2950_136-2949del
XM_005252822.3:c.61-99_61-98del	XP_005252879.1:n.61-99_61-98del
XM_005252823.3:c.58-99_58-98del	XP_005252880.1:n.58-99_58-98del
XM_011519949.1:c.88-2950_88-2949del	XP_011518251.1:n.88-2950_88-2949del
XM_005252820.3:c.139-2950_139-2949del	XP_005252877.2:n.139-2950_139-2949del
XM_005252821.3:c.136-2950_136-2949del	XP_005252878.2:n.136-2950_136-2949del
XM_005252822.4:c.61-99_61-98del	XP_005252879.1:n.61-99_61-98del
XM_011519949.2:c.88-2950_88-2949del	XP_011518251.1:n.88-2950_88-2949del
NM_001142649.2:c.136-99_136-98del	NP_001136121.1:n.136-99_136-98del
NM_213599.3:c.139-99_139-98del MANE Select	NP_998764.1:n.139-99_139-98del