Canonical Allele Identifier: CA1957395205

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22221158A= , CM000673.2:g.22221158A=	GRCh38
NC_000011.9:g.22242704A= , CM000673.1:g.22242704A=	GRCh37
NC_000011.8:g.22199280A=	NCBI36
NG_015844.1:g.32983A= , LRG_868:g.32983A=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.242A= MANE Select	NP_998764.1:p.Asp81=
ENST00000324559.9:c.242A= MANE Select	ENSP00000315371.9:p.Asp81=
NM_001142649.1:c.239A=	NP_001136121.1:p.Asp80=
NM_001142649.2:c.239A=	NP_001136121.1:p.Asp80=
NM_213599.2:c.242A= , LRG_868t1:c.242A=	NP_998764.1:p.Asp81=
ENST00000324559.8:c.242A=	ENSP00000315371.8:p.Asp81=
ENST00000648804.1:n.807A=
ENST00000682266.1:c.-209A=	ENSP00000507766.1:n.-209A=
ENST00000682341.1:c.200A=	ENSP00000508251.1:p.Asp67=
ENST00000682530.1:c.*174A=	ENSP00000506805.1:n.*174A=
ENST00000682684.1:n.621A=
ENST00000683197.1:c.200A=	ENSP00000507641.1:p.Asp67=
ENST00000683411.1:c.-209A=	ENSP00000508397.1:n.-209A=
ENST00000683437.1:c.-209A=	ENSP00000508408.1:n.-209A=
ENST00000683613.1:n.1236A=
ENST00000683834.1:n.442A=
ENST00000683897.1:n.486A=
ENST00000684365.1:n.611A=
ENST00000684663.1:c.197A=	ENSP00000508009.1:p.Asp66=
XM_005252820.2:c.200A=	XP_005252877.2:p.Asp67=
XM_005252820.3:c.200A=	XP_005252877.2:p.Asp67=
XM_005252821.2:c.197A=	XP_005252878.2:p.Asp66=
XM_005252821.3:c.197A=	XP_005252878.2:p.Asp66=
XM_005252822.3:c.164A=	XP_005252879.1:p.Asp55=
XM_005252822.4:c.164A=	XP_005252879.1:p.Asp55=
XM_005252823.3:c.161A=	XP_005252880.1:p.Asp54=
XM_011519949.1:c.149A=	XP_011518251.1:p.Asp50=
XM_011519949.2:c.149A=	XP_011518251.1:p.Asp50=