Canonical Allele Identifier: CA1957402780

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272831G= , CM000673.2:g.22272831G=	GRCh38
NC_000011.9:g.22294377G= , CM000673.1:g.22294377G=	GRCh37
NC_000011.8:g.22250953G=	NCBI36
NG_015844.1:g.84656G= , LRG_868:g.84656G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.94G=
ENST00000682266.1:c.1627G=	ENSP00000507766.1:p.Ala543=
ENST00000682341.1:c.2035G=	ENSP00000508251.1:p.Ala679=
ENST00000683197.1:c.2035G=	ENSP00000507641.1:p.Ala679=
ENST00000683411.1:c.1627G=	ENSP00000508397.1:p.Ala543=
ENST00000683437.1:c.1627G=	ENSP00000508408.1:p.Ala543=
ENST00000683613.1:n.3071G=
ENST00000684663.1:c.2032G=	ENSP00000508009.1:p.Ala678=
ENST00000324559.9:c.2077G= MANE Select	ENSP00000315371.9:p.Ala693=
ENST00000648804.1:n.2412G=
ENST00000324559.8:c.2077G=	ENSP00000315371.8:p.Ala693=
ENST00000532043.1:n.94G=
NM_001142649.1:c.2074G=	NP_001136121.1:p.Ala692=
NM_213599.2:c.2077G= , LRG_868t1:c.2077G=	NP_998764.1:p.Ala693=
XM_005252820.2:c.2035G=	XP_005252877.2:p.Ala679=
XM_005252821.2:c.2032G=	XP_005252878.2:p.Ala678=
XM_005252822.3:c.1999G=	XP_005252879.1:p.Ala667=
XM_005252823.3:c.1996G=	XP_005252880.1:p.Ala666=
XM_011519949.1:c.1984G=	XP_011518251.1:p.Ala662=
XM_005252820.3:c.2035G=	XP_005252877.2:p.Ala679=
XM_005252821.3:c.2032G=	XP_005252878.2:p.Ala678=
XM_005252822.4:c.1999G=	XP_005252879.1:p.Ala667=
XM_011519949.2:c.1984G=	XP_011518251.1:p.Ala662=
NM_001142649.2:c.2074G=	NP_001136121.1:p.Ala692=
NM_213599.3:c.2077G= MANE Select	NP_998764.1:p.Ala693=