Canonical Allele Identifier: CA473404193

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22271903A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250357A>G , CM000673.2:g.22250357A>G	GRCh38
NC_000011.9:g.22271903A>G , CM000673.1:g.22271903A>G	GRCh37
NC_000011.8:g.22228479A>G	NCBI36
NG_015844.1:g.62182A>G , LRG_868:g.62182A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.319A>G
ENST00000682266.1:c.549A>G	ENSP00000507766.1:p.Glu183=
ENST00000682341.1:c.957A>G	ENSP00000508251.1:p.Glu319=
ENST00000682530.1:c.*931A>G	ENSP00000506805.1:n.*931A>G
ENST00000683197.1:c.957A>G	ENSP00000507641.1:p.Glu319=
ENST00000683411.1:c.549A>G	ENSP00000508397.1:p.Glu183=
ENST00000683437.1:c.549A>G	ENSP00000508408.1:p.Glu183=
ENST00000683613.1:n.1993A>G
ENST00000683834.1:n.1199A>G
ENST00000684663.1:c.954A>G	ENSP00000508009.1:p.Glu318=
ENST00000324559.9:c.999A>G MANE Select	ENSP00000315371.9:p.Glu333=
ENST00000648804.1:n.1334A>G
ENST00000324559.8:c.999A>G	ENSP00000315371.8:p.Glu333=
NM_001142649.1:c.996A>G	NP_001136121.1:p.Glu332=
NM_213599.2:c.999A>G , LRG_868t1:c.999A>G	NP_998764.1:p.Glu333=
XM_005252820.2:c.957A>G	XP_005252877.2:p.Glu319=
XM_005252821.2:c.954A>G	XP_005252878.2:p.Glu318=
XM_005252822.3:c.921A>G	XP_005252879.1:p.Glu307=
XM_005252823.3:c.918A>G	XP_005252880.1:p.Glu306=
XM_011519949.1:c.906A>G	XP_011518251.1:p.Glu302=
XM_005252820.3:c.957A>G	XP_005252877.2:p.Glu319=
XM_005252821.3:c.954A>G	XP_005252878.2:p.Glu318=
XM_005252822.4:c.921A>G	XP_005252879.1:p.Glu307=
XM_011519949.2:c.906A>G	XP_011518251.1:p.Glu302=
NM_001142649.2:c.996A>G	NP_001136121.1:p.Glu332=
NM_213599.3:c.999A>G MANE Select	NP_998764.1:p.Glu333=