Canonical Allele Identifier: CA1957402957

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272894A= , CM000673.2:g.22272894A=	GRCh38
NC_000011.9:g.22294440A= , CM000673.1:g.22294440A=	GRCh37
NC_000011.8:g.22251016A=	NCBI36
NG_015844.1:g.84719A= , LRG_868:g.84719A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.157A=
ENST00000682266.1:c.1690A=	ENSP00000507766.1:p.Thr564=
ENST00000682341.1:c.2098A=	ENSP00000508251.1:p.Thr700=
ENST00000683197.1:c.2098A=	ENSP00000507641.1:p.Thr700=
ENST00000683411.1:c.1690A=	ENSP00000508397.1:p.Thr564=
ENST00000683437.1:c.1690A=	ENSP00000508408.1:p.Thr564=
ENST00000683613.1:n.3134A=
ENST00000684663.1:c.2095A=	ENSP00000508009.1:p.Thr699=
ENST00000324559.9:c.2140A= MANE Select	ENSP00000315371.9:p.Thr714=
ENST00000648804.1:n.2475A=
ENST00000324559.8:c.2140A=	ENSP00000315371.8:p.Thr714=
ENST00000532043.1:n.157A=
NM_001142649.1:c.2137A=	NP_001136121.1:p.Thr713=
NM_213599.2:c.2140A= , LRG_868t1:c.2140A=	NP_998764.1:p.Thr714=
XM_005252820.2:c.2098A=	XP_005252877.2:p.Thr700=
XM_005252821.2:c.2095A=	XP_005252878.2:p.Thr699=
XM_005252822.3:c.2062A=	XP_005252879.1:p.Thr688=
XM_005252823.3:c.2059A=	XP_005252880.1:p.Thr687=
XM_011519949.1:c.2047A=	XP_011518251.1:p.Thr683=
XM_005252820.3:c.2098A=	XP_005252877.2:p.Thr700=
XM_005252821.3:c.2095A=	XP_005252878.2:p.Thr699=
XM_005252822.4:c.2062A=	XP_005252879.1:p.Thr688=
XM_011519949.2:c.2047A=	XP_011518251.1:p.Thr683=
NM_001142649.2:c.2137A=	NP_001136121.1:p.Thr713=
NM_213599.3:c.2140A= MANE Select	NP_998764.1:p.Thr714=