Canonical Allele Identifier: CA2612864209

Gene: ANO5

Linked Data

• gnomAD v4: 11-22218115-T-TCTTACACACACACA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218116_22218117insTTACACACACACAC , CM000673.2:g.22218116_22218117insTTACACACACACAC	GRCh38
NC_000011.9:g.22239662_22239663insTTACACACACACAC , CM000673.1:g.22239662_22239663insTTACACACACACAC	GRCh37
NC_000011.8:g.22196238_22196239insTTACACACACACAC	NCBI36
NG_015844.1:g.29941_29942insTTACACACACACAC , LRG_868:g.29941_29942insTTACACACACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682084.1:n.3313-130_3313-129insTTACACACACACAC
ENST00000682266.1:c.-270-2981_-270-2980insTTACACACACACAC	ENSP00000507766.1:n.-270-2981_-270-2980insTTACACACACACAC
ENST00000682341.1:c.139-2981_139-2980insTTACACACACACAC	ENSP00000508251.1:n.139-2981_139-2980insTTACACACACACAC
ENST00000682530.1:c.136-627_136-626insTTACACACACACAC	ENSP00000506805.1:n.136-627_136-626insTTACACACACACAC
ENST00000682684.1:n.560-2981_560-2980insTTACACACACACAC
ENST00000683197.1:c.139-2981_139-2980insTTACACACACACAC	ENSP00000507641.1:n.139-2981_139-2980insTTACACACACACAC
ENST00000683411.1:c.-270-2981_-270-2980insTTACACACACACAC	ENSP00000508397.1:n.-270-2981_-270-2980insTTACACACACACAC
ENST00000683437.1:c.-270-2981_-270-2980insTTACACACACACAC	ENSP00000508408.1:n.-270-2981_-270-2980insTTACACACACACAC
ENST00000683834.1:n.381-2981_381-2980insTTACACACACACAC
ENST00000683897.1:n.425-2981_425-2980insTTACACACACACAC
ENST00000684365.1:n.550-2981_550-2980insTTACACACACACAC
ENST00000684663.1:c.136-2981_136-2980insTTACACACACACAC	ENSP00000508009.1:n.136-2981_136-2980insTTACACACACACAC
ENST00000324559.9:c.139-130_139-129insTTACACACACACAC MANE Select	ENSP00000315371.9:n.139-130_139-129insTTACACACACACAC
ENST00000648804.1:n.670-470_670-469insTTACACACACACAC
ENST00000324559.8:c.139-130_139-129insTTACACACACACAC	ENSP00000315371.8:n.139-130_139-129insTTACACACACACAC
NM_001142649.1:c.136-130_136-129insTTACACACACACAC	NP_001136121.1:n.136-130_136-129insTTACACACACACAC
NM_213599.2:c.139-130_139-129insTTACACACACACAC , LRG_868t1:c.139-130_139-129insTTACACACACACAC	NP_998764.1:n.139-130_139-129insTTACACACACACAC
XM_005252820.2:c.139-2981_139-2980insTTACACACACACAC	XP_005252877.2:n.139-2981_139-2980insTTACACACACACAC
XM_005252821.2:c.136-2981_136-2980insTTACACACACACAC	XP_005252878.2:n.136-2981_136-2980insTTACACACACACAC
XM_005252822.3:c.61-130_61-129insTTACACACACACAC	XP_005252879.1:n.61-130_61-129insTTACACACACACAC
XM_005252823.3:c.58-130_58-129insTTACACACACACAC	XP_005252880.1:n.58-130_58-129insTTACACACACACAC
XM_011519949.1:c.88-2981_88-2980insTTACACACACACAC	XP_011518251.1:n.88-2981_88-2980insTTACACACACACAC
XM_005252820.3:c.139-2981_139-2980insTTACACACACACAC	XP_005252877.2:n.139-2981_139-2980insTTACACACACACAC
XM_005252821.3:c.136-2981_136-2980insTTACACACACACAC	XP_005252878.2:n.136-2981_136-2980insTTACACACACACAC
XM_005252822.4:c.61-130_61-129insTTACACACACACAC	XP_005252879.1:n.61-130_61-129insTTACACACACACAC
XM_011519949.2:c.88-2981_88-2980insTTACACACACACAC	XP_011518251.1:n.88-2981_88-2980insTTACACACACACAC
NM_001142649.2:c.136-130_136-129insTTACACACACACAC	NP_001136121.1:n.136-130_136-129insTTACACACACACAC
NM_213599.3:c.139-130_139-129insTTACACACACACAC MANE Select	NP_998764.1:n.139-130_139-129insTTACACACACACAC