Canonical Allele Identifier: CA218756268

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22193773C>A , CM000673.2:g.22193773C>A	GRCh38
NC_000011.9:g.22215319C>A , CM000673.1:g.22215319C>A	GRCh37
NC_000011.8:g.22171895C>A	NCBI36
NG_015844.1:g.5598C>A , LRG_868:g.5598C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.-322+241C>A	ENSP00000507766.1:n.-322+241C>A
ENST00000682341.1:c.40+241C>A	ENSP00000508251.1:n.40+241C>A
ENST00000682530.1:c.40+241C>A	ENSP00000506805.1:n.40+241C>A
ENST00000682684.1:n.464+241C>A
ENST00000683197.1:c.40+241C>A	ENSP00000507641.1:n.40+241C>A
ENST00000683411.1:c.-383+241C>A	ENSP00000508397.1:n.-383+241C>A
ENST00000683437.1:c.-271+241C>A	ENSP00000508408.1:n.-271+241C>A
ENST00000683834.1:n.285+241C>A
ENST00000683897.1:n.326+241C>A
ENST00000684365.1:n.454+241C>A
ENST00000684663.1:c.40+241C>A	ENSP00000508009.1:n.40+241C>A
ENST00000324559.9:c.40+241C>A MANE Select	ENSP00000315371.9:n.40+241C>A
ENST00000648804.1:n.545-10031C>A
ENST00000324559.8:c.40+241C>A	ENSP00000315371.8:n.40+241C>A
NM_001142649.1:c.40+241C>A	NP_001136121.1:n.40+241C>A
NM_213599.2:c.40+241C>A , LRG_868t1:c.40+241C>A	NP_998764.1:n.40+241C>A
XM_005252820.2:c.40+241C>A	XP_005252877.2:n.40+241C>A
XM_005252821.2:c.40+241C>A	XP_005252878.2:n.40+241C>A
XM_005252822.3:c.-39+1047C>A	XP_005252879.1:n.-39+1047C>A
XM_005252823.3:c.-39+1047C>A	XP_005252880.1:n.-39+1047C>A
XM_011519949.1:c.40+241C>A	XP_011518251.1:n.40+241C>A
XM_005252820.3:c.40+241C>A	XP_005252877.2:n.40+241C>A
XM_005252821.3:c.40+241C>A	XP_005252878.2:n.40+241C>A
XM_005252822.4:c.-39+1047C>A	XP_005252879.1:n.-39+1047C>A
XM_011519949.2:c.40+241C>A	XP_011518251.1:n.40+241C>A
NM_001142649.2:c.40+241C>A	NP_001136121.1:n.40+241C>A
NM_213599.3:c.40+241C>A MANE Select	NP_998764.1:n.40+241C>A