Canonical Allele Identifier: CA1957386695

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22203803G= , CM000673.2:g.22203803G=	GRCh38
NC_000011.9:g.22225349G= , CM000673.1:g.22225349G=	GRCh37
NC_000011.8:g.22181925G=	NCBI36
NG_015844.1:g.15628G= , LRG_868:g.15628G=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.41-1G= MANE Select	NP_998764.1:n.41-1G=
ENST00000324559.9:c.41-1G= MANE Select	ENSP00000315371.9:n.41-1G=
NM_001142649.1:c.41-1G=	NP_001136121.1:n.41-1G=
NM_001142649.2:c.41-1G=	NP_001136121.1:n.41-1G=
NM_213599.2:c.41-1G= , LRG_868t1:c.41-1G=	NP_998764.1:n.41-1G=
ENST00000324559.8:c.41-1G=	ENSP00000315371.8:n.41-1G=
ENST00000648804.1:n.545-1G=
ENST00000682266.1:c.-321-7461G=	ENSP00000507766.1:n.-321-7461G=
ENST00000682341.1:c.41-1G=	ENSP00000508251.1:n.41-1G=
ENST00000682530.1:c.41-1G=	ENSP00000506805.1:n.41-1G=
ENST00000682684.1:n.465-1G=
ENST00000683197.1:c.41-1G=	ENSP00000507641.1:n.41-1G=
ENST00000683411.1:c.-382-7461G=	ENSP00000508397.1:n.-382-7461G=
ENST00000683437.1:c.-271+10271G=	ENSP00000508408.1:n.-271+10271G=
ENST00000683834.1:n.286-1G=
ENST00000683897.1:n.327-1G=
ENST00000684365.1:n.455-1G=
ENST00000684663.1:c.41-1G=	ENSP00000508009.1:n.41-1G=
XM_005252820.2:c.41-1G=	XP_005252877.2:n.41-1G=
XM_005252820.3:c.41-1G=	XP_005252877.2:n.41-1G=
XM_005252821.2:c.41-1G=	XP_005252878.2:n.41-1G=
XM_005252821.3:c.41-1G=	XP_005252878.2:n.41-1G=
XM_005252822.3:c.-38-1G=	XP_005252879.1:n.-38-1G=
XM_005252822.4:c.-38-1G=	XP_005252879.1:n.-38-1G=
XM_005252823.3:c.-38-1G=	XP_005252880.1:n.-38-1G=
XM_011519949.1:c.41-1G=	XP_011518251.1:n.41-1G=
XM_011519949.2:c.41-1G=	XP_011518251.1:n.41-1G=