Canonical Allele Identifier: CA473405081

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22281193A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259647A>T , CM000673.2:g.22259647A>T	GRCh38
NC_000011.9:g.22281193A>T , CM000673.1:g.22281193A>T	GRCh37
NC_000011.8:g.22237769A>T	NCBI36
NG_015844.1:g.71472A>T , LRG_868:g.71472A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1086A>T	ENSP00000507766.1:p.Ile362=
ENST00000682341.1:c.1494A>T	ENSP00000508251.1:p.Ile498=
ENST00000683197.1:c.1494A>T	ENSP00000507641.1:p.Ile498=
ENST00000683411.1:c.1086A>T	ENSP00000508397.1:p.Ile362=
ENST00000683437.1:c.1086A>T	ENSP00000508408.1:p.Ile362=
ENST00000683613.1:n.2530A>T
ENST00000684663.1:c.1491A>T	ENSP00000508009.1:p.Ile497=
ENST00000324559.9:c.1536A>T MANE Select	ENSP00000315371.9:p.Ile512=
ENST00000648804.1:n.1871A>T
ENST00000324559.8:c.1536A>T	ENSP00000315371.8:p.Ile512=
NM_001142649.1:c.1533A>T	NP_001136121.1:p.Ile511=
NM_213599.2:c.1536A>T , LRG_868t1:c.1536A>T	NP_998764.1:p.Ile512=
XM_005252820.2:c.1494A>T	XP_005252877.2:p.Ile498=
XM_005252821.2:c.1491A>T	XP_005252878.2:p.Ile497=
XM_005252822.3:c.1458A>T	XP_005252879.1:p.Ile486=
XM_005252823.3:c.1455A>T	XP_005252880.1:p.Ile485=
XM_011519949.1:c.1443A>T	XP_011518251.1:p.Ile481=
XM_005252820.3:c.1494A>T	XP_005252877.2:p.Ile498=
XM_005252821.3:c.1491A>T	XP_005252878.2:p.Ile497=
XM_005252822.4:c.1458A>T	XP_005252879.1:p.Ile486=
XM_011519949.2:c.1443A>T	XP_011518251.1:p.Ile481=
NM_001142649.2:c.1533A>T	NP_001136121.1:p.Ile511=
NM_213599.3:c.1536A>T MANE Select	NP_998764.1:p.Ile512=