Canonical Allele Identifier: CA379921459

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22276967G>T (hg19) ; chr11:g.22255421G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255421G>T , CM000673.2:g.22255421G>T	GRCh38
NC_000011.9:g.22276967G>T , CM000673.1:g.22276967G>T	GRCh37
NC_000011.8:g.22233543G>T	NCBI36
NG_015844.1:g.67246G>T , LRG_868:g.67246G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.551G>T
ENST00000682266.1:c.781G>T	ENSP00000507766.1:p.Glu261Ter
ENST00000682341.1:c.1189G>T	ENSP00000508251.1:p.Glu397Ter
ENST00000682530.1:c.*1163G>T	ENSP00000506805.1:n.*1163G>T
ENST00000683197.1:c.1189G>T	ENSP00000507641.1:p.Glu397Ter
ENST00000683411.1:c.781G>T	ENSP00000508397.1:p.Glu261Ter
ENST00000683437.1:c.781G>T	ENSP00000508408.1:p.Glu261Ter
ENST00000683613.1:n.2225G>T
ENST00000683834.1:n.1431G>T
ENST00000684663.1:c.1186G>T	ENSP00000508009.1:p.Glu396Ter
ENST00000324559.9:c.1231G>T MANE Select	ENSP00000315371.9:p.Glu411Ter
ENST00000648804.1:n.1566G>T
ENST00000324559.8:c.1231G>T	ENSP00000315371.8:p.Glu411Ter
NM_001142649.1:c.1228G>T	NP_001136121.1:p.Glu410Ter
NM_213599.2:c.1231G>T , LRG_868t1:c.1231G>T	NP_998764.1:p.Glu411Ter
XM_005252820.2:c.1189G>T	XP_005252877.2:p.Glu397Ter
XM_005252821.2:c.1186G>T	XP_005252878.2:p.Glu396Ter
XM_005252822.3:c.1153G>T	XP_005252879.1:p.Glu385Ter
XM_005252823.3:c.1150G>T	XP_005252880.1:p.Glu384Ter
XM_011519949.1:c.1138G>T	XP_011518251.1:p.Glu380Ter
XM_005252820.3:c.1189G>T	XP_005252877.2:p.Glu397Ter
XM_005252821.3:c.1186G>T	XP_005252878.2:p.Glu396Ter
XM_005252822.4:c.1153G>T	XP_005252879.1:p.Glu385Ter
XM_011519949.2:c.1138G>T	XP_011518251.1:p.Glu380Ter
NM_001142649.2:c.1228G>T	NP_001136121.1:p.Glu410Ter
NM_213599.3:c.1231G>T MANE Select	NP_998764.1:p.Glu411Ter