Canonical Allele Identifier: CA1957403100

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272947A= , CM000673.2:g.22272947A=	GRCh38
NC_000011.9:g.22294493A= , CM000673.1:g.22294493A=	GRCh37
NC_000011.8:g.22251069A=	NCBI36
NG_015844.1:g.84772A= , LRG_868:g.84772A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.210A=
ENST00000682266.1:c.1743A=	ENSP00000507766.1:p.Gln581=
ENST00000682341.1:c.2151A=	ENSP00000508251.1:p.Gln717=
ENST00000683197.1:c.2151A=	ENSP00000507641.1:p.Gln717=
ENST00000683411.1:c.1743A=	ENSP00000508397.1:p.Gln581=
ENST00000683437.1:c.1743A=	ENSP00000508408.1:p.Gln581=
ENST00000683613.1:n.3187A=
ENST00000684663.1:c.2148A=	ENSP00000508009.1:p.Gln716=
ENST00000324559.9:c.2193A= MANE Select	ENSP00000315371.9:p.Gln731=
ENST00000648804.1:n.2528A=
ENST00000324559.8:c.2193A=	ENSP00000315371.8:p.Gln731=
ENST00000532043.1:n.210A=
NM_001142649.1:c.2190A=	NP_001136121.1:p.Gln730=
NM_213599.2:c.2193A= , LRG_868t1:c.2193A=	NP_998764.1:p.Gln731=
XM_005252820.2:c.2151A=	XP_005252877.2:p.Gln717=
XM_005252821.2:c.2148A=	XP_005252878.2:p.Gln716=
XM_005252822.3:c.2115A=	XP_005252879.1:p.Gln705=
XM_005252823.3:c.2112A=	XP_005252880.1:p.Gln704=
XM_011519949.1:c.2100A=	XP_011518251.1:p.Gln700=
XM_005252820.3:c.2151A=	XP_005252877.2:p.Gln717=
XM_005252821.3:c.2148A=	XP_005252878.2:p.Gln716=
XM_005252822.4:c.2115A=	XP_005252879.1:p.Gln705=
XM_011519949.2:c.2100A=	XP_011518251.1:p.Gln700=
NM_001142649.2:c.2190A=	NP_001136121.1:p.Gln730=
NM_213599.3:c.2193A= MANE Select	NP_998764.1:p.Gln731=