Canonical Allele Identifier: CA1957418643

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259372G= , CM000673.2:g.22259372G=	GRCh38
NC_000011.9:g.22280918G= , CM000673.1:g.22280918G=	GRCh37
NC_000011.8:g.22237494G=	NCBI36
NG_015844.1:g.71197G= , LRG_868:g.71197G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.958-147G=	ENSP00000507766.1:n.958-147G=
ENST00000682341.1:c.1366-147G=	ENSP00000508251.1:n.1366-147G=
ENST00000683197.1:c.1366-147G=	ENSP00000507641.1:n.1366-147G=
ENST00000683411.1:c.958-147G=	ENSP00000508397.1:n.958-147G=
ENST00000683437.1:c.958-147G=	ENSP00000508408.1:n.958-147G=
ENST00000683613.1:n.2402-147G=
ENST00000684663.1:c.1363-147G=	ENSP00000508009.1:n.1363-147G=
ENST00000324559.9:c.1408-147G= MANE Select	ENSP00000315371.9:n.1408-147G=
ENST00000648804.1:n.1743-147G=
ENST00000324559.8:c.1408-147G=	ENSP00000315371.8:n.1408-147G=
NM_001142649.1:c.1405-147G=	NP_001136121.1:n.1405-147G=
NM_213599.2:c.1408-147G= , LRG_868t1:c.1408-147G=	NP_998764.1:n.1408-147G=
XM_005252820.2:c.1366-147G=	XP_005252877.2:n.1366-147G=
XM_005252821.2:c.1363-147G=	XP_005252878.2:n.1363-147G=
XM_005252822.3:c.1330-147G=	XP_005252879.1:n.1330-147G=
XM_005252823.3:c.1327-147G=	XP_005252880.1:n.1327-147G=
XM_011519949.1:c.1315-147G=	XP_011518251.1:n.1315-147G=
XM_005252820.3:c.1366-147G=	XP_005252877.2:n.1366-147G=
XM_005252821.3:c.1363-147G=	XP_005252878.2:n.1363-147G=
XM_005252822.4:c.1330-147G=	XP_005252879.1:n.1330-147G=
XM_011519949.2:c.1315-147G=	XP_011518251.1:n.1315-147G=
NM_001142649.2:c.1405-147G=	NP_001136121.1:n.1405-147G=
NM_213599.3:c.1408-147G= MANE Select	NP_998764.1:n.1408-147G=