Canonical Allele Identifier: CA1957413239

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250348A= , CM000673.2:g.22250348A=	GRCh38
NC_000011.9:g.22271894A= , CM000673.1:g.22271894A=	GRCh37
NC_000011.8:g.22228470A=	NCBI36
NG_015844.1:g.62173A= , LRG_868:g.62173A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.310A=
ENST00000682266.1:c.540A=	ENSP00000507766.1:p.Leu180=
ENST00000682341.1:c.948A=	ENSP00000508251.1:p.Leu316=
ENST00000682530.1:c.*922A=	ENSP00000506805.1:n.*922A=
ENST00000683197.1:c.948A=	ENSP00000507641.1:p.Leu316=
ENST00000683411.1:c.540A=	ENSP00000508397.1:p.Leu180=
ENST00000683437.1:c.540A=	ENSP00000508408.1:p.Leu180=
ENST00000683613.1:n.1984A=
ENST00000683834.1:n.1190A=
ENST00000684663.1:c.945A=	ENSP00000508009.1:p.Leu315=
ENST00000324559.9:c.990A= MANE Select	ENSP00000315371.9:p.Leu330=
ENST00000648804.1:n.1325A=
ENST00000324559.8:c.990A=	ENSP00000315371.8:p.Leu330=
NM_001142649.1:c.987A=	NP_001136121.1:p.Leu329=
NM_213599.2:c.990A= , LRG_868t1:c.990A=	NP_998764.1:p.Leu330=
XM_005252820.2:c.948A=	XP_005252877.2:p.Leu316=
XM_005252821.2:c.945A=	XP_005252878.2:p.Leu315=
XM_005252822.3:c.912A=	XP_005252879.1:p.Leu304=
XM_005252823.3:c.909A=	XP_005252880.1:p.Leu303=
XM_011519949.1:c.897A=	XP_011518251.1:p.Leu299=
XM_005252820.3:c.948A=	XP_005252877.2:p.Leu316=
XM_005252821.3:c.945A=	XP_005252878.2:p.Leu315=
XM_005252822.4:c.912A=	XP_005252879.1:p.Leu304=
XM_011519949.2:c.897A=	XP_011518251.1:p.Leu299=
NM_001142649.2:c.987A=	NP_001136121.1:p.Leu329=
NM_213599.3:c.990A= MANE Select	NP_998764.1:p.Leu330=