Canonical Allele Identifier: CA2612864841

Gene: ANO5

Linked Data

• gnomAD v4: 11-22225841-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22225841_22225842insA , CM000673.2:g.22225841_22225842insA	GRCh38
NC_000011.9:g.22247387_22247388insA , CM000673.1:g.22247387_22247388insA	GRCh37
NC_000011.8:g.22203963_22203964insA	NCBI36
NG_015844.1:g.37666_37667insA , LRG_868:g.37666_37667insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.-156-143_-156-142insA	ENSP00000507766.1:n.-156-143_-156-142insA
ENST00000682341.1:c.253-143_253-142insA	ENSP00000508251.1:n.253-143_253-142insA
ENST00000682530.1:c.*227-143_*227-142insA	ENSP00000506805.1:n.*227-143_*227-142insA
ENST00000682684.1:n.674-143_674-142insA
ENST00000683197.1:c.253-143_253-142insA	ENSP00000507641.1:n.253-143_253-142insA
ENST00000683411.1:c.-156-143_-156-142insA	ENSP00000508397.1:n.-156-143_-156-142insA
ENST00000683437.1:c.-156-143_-156-142insA	ENSP00000508408.1:n.-156-143_-156-142insA
ENST00000683613.1:n.1289-143_1289-142insA
ENST00000683834.1:n.495-143_495-142insA
ENST00000684663.1:c.250-143_250-142insA	ENSP00000508009.1:n.250-143_250-142insA
ENST00000324559.9:c.295-143_295-142insA MANE Select	ENSP00000315371.9:n.295-143_295-142insA
ENST00000648804.1:n.860-143_860-142insA
ENST00000324559.8:c.295-143_295-142insA	ENSP00000315371.8:n.295-143_295-142insA
NM_001142649.1:c.292-143_292-142insA	NP_001136121.1:n.292-143_292-142insA
NM_213599.2:c.295-143_295-142insA , LRG_868t1:c.295-143_295-142insA	NP_998764.1:n.295-143_295-142insA
XM_005252820.2:c.253-143_253-142insA	XP_005252877.2:n.253-143_253-142insA
XM_005252821.2:c.250-143_250-142insA	XP_005252878.2:n.250-143_250-142insA
XM_005252822.3:c.217-143_217-142insA	XP_005252879.1:n.217-143_217-142insA
XM_005252823.3:c.214-143_214-142insA	XP_005252880.1:n.214-143_214-142insA
XM_011519949.1:c.202-143_202-142insA	XP_011518251.1:n.202-143_202-142insA
XM_005252820.3:c.253-143_253-142insA	XP_005252877.2:n.253-143_253-142insA
XM_005252821.3:c.250-143_250-142insA	XP_005252878.2:n.250-143_250-142insA
XM_005252822.4:c.217-143_217-142insA	XP_005252879.1:n.217-143_217-142insA
XM_011519949.2:c.202-143_202-142insA	XP_011518251.1:n.202-143_202-142insA
NM_001142649.2:c.292-143_292-142insA	NP_001136121.1:n.292-143_292-142insA
NM_213599.3:c.295-143_295-142insA MANE Select	NP_998764.1:n.295-143_295-142insA