Canonical Allele Identifier: CA1957420197

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262982C= , CM000673.2:g.22262982C=	GRCh38
NC_000011.9:g.22284528C= , CM000673.1:g.22284528C=	GRCh37
NC_000011.8:g.22241104C=	NCBI36
NG_015844.1:g.74807C= , LRG_868:g.74807C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1387C=	ENSP00000507766.1:p.Gln463=
ENST00000682341.1:c.1795C=	ENSP00000508251.1:p.Gln599=
ENST00000683197.1:c.1795C=	ENSP00000507641.1:p.Gln599=
ENST00000683411.1:c.1387C=	ENSP00000508397.1:p.Gln463=
ENST00000683437.1:c.1387C=	ENSP00000508408.1:p.Gln463=
ENST00000683613.1:n.2831C=
ENST00000684663.1:c.1792C=	ENSP00000508009.1:p.Gln598=
ENST00000324559.9:c.1837C= MANE Select	ENSP00000315371.9:p.Gln613=
ENST00000648804.1:n.2172C=
ENST00000324559.8:c.1837C=	ENSP00000315371.8:p.Gln613=
NM_001142649.1:c.1834C=	NP_001136121.1:p.Gln612=
NM_213599.2:c.1837C= , LRG_868t1:c.1837C=	NP_998764.1:p.Gln613=
XM_005252820.2:c.1795C=	XP_005252877.2:p.Gln599=
XM_005252821.2:c.1792C=	XP_005252878.2:p.Gln598=
XM_005252822.3:c.1759C=	XP_005252879.1:p.Gln587=
XM_005252823.3:c.1756C=	XP_005252880.1:p.Gln586=
XM_011519949.1:c.1744C=	XP_011518251.1:p.Gln582=
XM_005252820.3:c.1795C=	XP_005252877.2:p.Gln599=
XM_005252821.3:c.1792C=	XP_005252878.2:p.Gln598=
XM_005252822.4:c.1759C=	XP_005252879.1:p.Gln587=
XM_011519949.2:c.1744C=	XP_011518251.1:p.Gln582=
NM_001142649.2:c.1834C=	NP_001136121.1:p.Gln612=
NM_213599.3:c.1837C= MANE Select	NP_998764.1:p.Gln613=