Canonical Allele Identifier: CA473405006

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22281109C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259563C>T , CM000673.2:g.22259563C>T	GRCh38
NC_000011.9:g.22281109C>T , CM000673.1:g.22281109C>T	GRCh37
NC_000011.8:g.22237685C>T	NCBI36
NG_015844.1:g.71388C>T , LRG_868:g.71388C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1002C>T	ENSP00000507766.1:p.Arg334=
ENST00000682341.1:c.1410C>T	ENSP00000508251.1:p.Arg470=
ENST00000683197.1:c.1410C>T	ENSP00000507641.1:p.Arg470=
ENST00000683411.1:c.1002C>T	ENSP00000508397.1:p.Arg334=
ENST00000683437.1:c.1002C>T	ENSP00000508408.1:p.Arg334=
ENST00000683613.1:n.2446C>T
ENST00000684663.1:c.1407C>T	ENSP00000508009.1:p.Arg469=
ENST00000324559.9:c.1452C>T MANE Select	ENSP00000315371.9:p.Arg484=
ENST00000648804.1:n.1787C>T
ENST00000324559.8:c.1452C>T	ENSP00000315371.8:p.Arg484=
NM_001142649.1:c.1449C>T	NP_001136121.1:p.Arg483=
NM_213599.2:c.1452C>T , LRG_868t1:c.1452C>T	NP_998764.1:p.Arg484=
XM_005252820.2:c.1410C>T	XP_005252877.2:p.Arg470=
XM_005252821.2:c.1407C>T	XP_005252878.2:p.Arg469=
XM_005252822.3:c.1374C>T	XP_005252879.1:p.Arg458=
XM_005252823.3:c.1371C>T	XP_005252880.1:p.Arg457=
XM_011519949.1:c.1359C>T	XP_011518251.1:p.Arg453=
XM_005252820.3:c.1410C>T	XP_005252877.2:p.Arg470=
XM_005252821.3:c.1407C>T	XP_005252878.2:p.Arg469=
XM_005252822.4:c.1374C>T	XP_005252879.1:p.Arg458=
XM_011519949.2:c.1359C>T	XP_011518251.1:p.Arg453=
NM_001142649.2:c.1449C>T	NP_001136121.1:p.Arg483=
NM_213599.3:c.1452C>T MANE Select	NP_998764.1:p.Arg484=