Canonical Allele Identifier: CA379920621

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22239685G>A , CM000673.2:g.22239685G>A	GRCh38
NC_000011.9:g.22261231G>A , CM000673.1:g.22261231G>A	GRCh37
NC_000011.8:g.22217807G>A	NCBI36
NG_015844.1:g.51510G>A , LRG_868:g.51510G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.878+1G>A MANE Select	NP_998764.1:n.878+1G>A
ENST00000324559.9:c.878+1G>A MANE Select	ENSP00000315371.9:n.878+1G>A
NM_001142649.1:c.875+1G>A	NP_001136121.1:n.875+1G>A
NM_001142649.2:c.875+1G>A	NP_001136121.1:n.875+1G>A
NM_213599.2:c.878+1G>A , LRG_868t1:c.878+1G>A	NP_998764.1:n.878+1G>A
ENST00000324559.8:c.878+1G>A	ENSP00000315371.8:n.878+1G>A
ENST00000648804.1:n.1214-10552G>A
ENST00000682266.1:c.428+1G>A	ENSP00000507766.1:n.428+1G>A
ENST00000682341.1:c.836+1G>A	ENSP00000508251.1:n.836+1G>A
ENST00000682530.1:c.*810+1G>A	ENSP00000506805.1:n.*810+1G>A
ENST00000682684.1:n.1257+1G>A
ENST00000683197.1:c.836+1G>A	ENSP00000507641.1:n.836+1G>A
ENST00000683411.1:c.428+1G>A	ENSP00000508397.1:n.428+1G>A
ENST00000683437.1:c.428+1G>A	ENSP00000508408.1:n.428+1G>A
ENST00000683613.1:n.1872+1G>A
ENST00000683834.1:n.1078+1G>A
ENST00000684663.1:c.833+1G>A	ENSP00000508009.1:n.833+1G>A
XM_005252820.2:c.836+1G>A	XP_005252877.2:n.836+1G>A
XM_005252820.3:c.836+1G>A	XP_005252877.2:n.836+1G>A
XM_005252821.2:c.833+1G>A	XP_005252878.2:n.833+1G>A
XM_005252821.3:c.833+1G>A	XP_005252878.2:n.833+1G>A
XM_005252822.3:c.800+1G>A	XP_005252879.1:n.800+1G>A
XM_005252822.4:c.800+1G>A	XP_005252879.1:n.800+1G>A
XM_005252823.3:c.797+1G>A	XP_005252880.1:n.797+1G>A
XM_011519949.1:c.785+1G>A	XP_011518251.1:n.785+1G>A
XM_011519949.2:c.785+1G>A	XP_011518251.1:n.785+1G>A