Canonical Allele Identifier: CA379920492

Gene: ANO5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22239629C>T , CM000673.2:g.22239629C>T	GRCh38
NC_000011.9:g.22261175C>T , CM000673.1:g.22261175C>T	GRCh37
NC_000011.8:g.22217751C>T	NCBI36
NG_015844.1:g.51454C>T , LRG_868:g.51454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.373C>T	ENSP00000507766.1:p.Gln125Ter
ENST00000682341.1:c.781C>T	ENSP00000508251.1:p.Gln261Ter
ENST00000682530.1:c.*755C>T	ENSP00000506805.1:n.*755C>T
ENST00000682684.1:n.1202C>T
ENST00000683197.1:c.781C>T	ENSP00000507641.1:p.Gln261Ter
ENST00000683411.1:c.373C>T	ENSP00000508397.1:p.Gln125Ter
ENST00000683437.1:c.373C>T	ENSP00000508408.1:p.Gln125Ter
ENST00000683613.1:n.1817C>T
ENST00000683834.1:n.1023C>T
ENST00000684663.1:c.778C>T	ENSP00000508009.1:p.Gln260Ter
ENST00000324559.9:c.823C>T MANE Select	ENSP00000315371.9:p.Gln275Ter
ENST00000648804.1:n.1214-10608C>T
ENST00000324559.8:c.823C>T	ENSP00000315371.8:p.Gln275Ter
NM_001142649.1:c.820C>T	NP_001136121.1:p.Gln274Ter
NM_213599.2:c.823C>T , LRG_868t1:c.823C>T	NP_998764.1:p.Gln275Ter
XM_005252820.2:c.781C>T	XP_005252877.2:p.Gln261Ter
XM_005252821.2:c.778C>T	XP_005252878.2:p.Gln260Ter
XM_005252822.3:c.745C>T	XP_005252879.1:p.Gln249Ter
XM_005252823.3:c.742C>T	XP_005252880.1:p.Gln248Ter
XM_011519949.1:c.730C>T	XP_011518251.1:p.Gln244Ter
XM_005252820.3:c.781C>T	XP_005252877.2:p.Gln261Ter
XM_005252821.3:c.778C>T	XP_005252878.2:p.Gln260Ter
XM_005252822.4:c.745C>T	XP_005252879.1:p.Gln249Ter
XM_011519949.2:c.730C>T	XP_011518251.1:p.Gln244Ter
NM_001142649.2:c.820C>T	NP_001136121.1:p.Gln274Ter
NM_213599.3:c.823C>T MANE Select	NP_998764.1:p.Gln275Ter