Canonical Allele Identifier: CA379922241

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22281190G>T (hg19) ; chr11:g.22259644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259644G>T , CM000673.2:g.22259644G>T	GRCh38
NC_000011.9:g.22281190G>T , CM000673.1:g.22281190G>T	GRCh37
NC_000011.8:g.22237766G>T	NCBI36
NG_015844.1:g.71469G>T , LRG_868:g.71469G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1083G>T	ENSP00000507766.1:p.Gln361His
ENST00000682341.1:c.1491G>T	ENSP00000508251.1:p.Gln497His
ENST00000683197.1:c.1491G>T	ENSP00000507641.1:p.Gln497His
ENST00000683411.1:c.1083G>T	ENSP00000508397.1:p.Gln361His
ENST00000683437.1:c.1083G>T	ENSP00000508408.1:p.Gln361His
ENST00000683613.1:n.2527G>T
ENST00000684663.1:c.1488G>T	ENSP00000508009.1:p.Gln496His
ENST00000324559.9:c.1533G>T MANE Select	ENSP00000315371.9:p.Gln511His
ENST00000648804.1:n.1868G>T
ENST00000324559.8:c.1533G>T	ENSP00000315371.8:p.Gln511His
NM_001142649.1:c.1530G>T	NP_001136121.1:p.Gln510His
NM_213599.2:c.1533G>T , LRG_868t1:c.1533G>T	NP_998764.1:p.Gln511His
XM_005252820.2:c.1491G>T	XP_005252877.2:p.Gln497His
XM_005252821.2:c.1488G>T	XP_005252878.2:p.Gln496His
XM_005252822.3:c.1455G>T	XP_005252879.1:p.Gln485His
XM_005252823.3:c.1452G>T	XP_005252880.1:p.Gln484His
XM_011519949.1:c.1440G>T	XP_011518251.1:p.Gln480His
XM_005252820.3:c.1491G>T	XP_005252877.2:p.Gln497His
XM_005252821.3:c.1488G>T	XP_005252878.2:p.Gln496His
XM_005252822.4:c.1455G>T	XP_005252879.1:p.Gln485His
XM_011519949.2:c.1440G>T	XP_011518251.1:p.Gln480His
NM_001142649.2:c.1530G>T	NP_001136121.1:p.Gln510His
NM_213599.3:c.1533G>T MANE Select	NP_998764.1:p.Gln511His