Canonical Allele Identifier: CA1957417929

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22257753G= , CM000673.2:g.22257753G=	GRCh38
NC_000011.9:g.22279299G= , CM000673.1:g.22279299G=	GRCh37
NC_000011.8:g.22235875G=	NCBI36
NG_015844.1:g.69578G= , LRG_868:g.69578G=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1406G= MANE Select	NP_998764.1:p.Trp469=
ENST00000324559.9:c.1406G= MANE Select	ENSP00000315371.9:p.Trp469=
NM_001142649.1:c.1403G=	NP_001136121.1:p.Trp468=
NM_001142649.2:c.1403G=	NP_001136121.1:p.Trp468=
NM_213599.2:c.1406G= , LRG_868t1:c.1406G=	NP_998764.1:p.Trp469=
ENST00000324559.8:c.1406G=	ENSP00000315371.8:p.Trp469=
ENST00000648804.1:n.1741G=
ENST00000682266.1:c.956G=	ENSP00000507766.1:p.Trp319=
ENST00000682341.1:c.1364G=	ENSP00000508251.1:p.Trp455=
ENST00000683197.1:c.1364G=	ENSP00000507641.1:p.Trp455=
ENST00000683411.1:c.956G=	ENSP00000508397.1:p.Trp319=
ENST00000683437.1:c.956G=	ENSP00000508408.1:p.Trp319=
ENST00000683613.1:n.2400G=
ENST00000684663.1:c.1361G=	ENSP00000508009.1:p.Trp454=
XM_005252820.2:c.1364G=	XP_005252877.2:p.Trp455=
XM_005252820.3:c.1364G=	XP_005252877.2:p.Trp455=
XM_005252821.2:c.1361G=	XP_005252878.2:p.Trp454=
XM_005252821.3:c.1361G=	XP_005252878.2:p.Trp454=
XM_005252822.3:c.1328G=	XP_005252879.1:p.Trp443=
XM_005252822.4:c.1328G=	XP_005252879.1:p.Trp443=
XM_005252823.3:c.1325G=	XP_005252880.1:p.Trp442=
XM_011519949.1:c.1313G=	XP_011518251.1:p.Trp438=
XM_011519949.2:c.1313G=	XP_011518251.1:p.Trp438=