Canonical Allele Identifier: CA1957403083

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272931G= , CM000673.2:g.22272931G=	GRCh38
NC_000011.9:g.22294477G= , CM000673.1:g.22294477G=	GRCh37
NC_000011.8:g.22251053G=	NCBI36
NG_015844.1:g.84756G= , LRG_868:g.84756G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.194G=
ENST00000682266.1:c.1727G=	ENSP00000507766.1:p.Ser576=
ENST00000682341.1:c.2135G=	ENSP00000508251.1:p.Ser712=
ENST00000683197.1:c.2135G=	ENSP00000507641.1:p.Ser712=
ENST00000683411.1:c.1727G=	ENSP00000508397.1:p.Ser576=
ENST00000683437.1:c.1727G=	ENSP00000508408.1:p.Ser576=
ENST00000683613.1:n.3171G=
ENST00000684663.1:c.2132G=	ENSP00000508009.1:p.Ser711=
ENST00000324559.9:c.2177G= MANE Select	ENSP00000315371.9:p.Ser726=
ENST00000648804.1:n.2512G=
ENST00000324559.8:c.2177G=	ENSP00000315371.8:p.Ser726=
ENST00000532043.1:n.194G=
NM_001142649.1:c.2174G=	NP_001136121.1:p.Ser725=
NM_213599.2:c.2177G= , LRG_868t1:c.2177G=	NP_998764.1:p.Ser726=
XM_005252820.2:c.2135G=	XP_005252877.2:p.Ser712=
XM_005252821.2:c.2132G=	XP_005252878.2:p.Ser711=
XM_005252822.3:c.2099G=	XP_005252879.1:p.Ser700=
XM_005252823.3:c.2096G=	XP_005252880.1:p.Ser699=
XM_011519949.1:c.2084G=	XP_011518251.1:p.Ser695=
XM_005252820.3:c.2135G=	XP_005252877.2:p.Ser712=
XM_005252821.3:c.2132G=	XP_005252878.2:p.Ser711=
XM_005252822.4:c.2099G=	XP_005252879.1:p.Ser700=
XM_011519949.2:c.2084G=	XP_011518251.1:p.Ser695=
NM_001142649.2:c.2174G=	NP_001136121.1:p.Ser725=
NM_213599.3:c.2177G= MANE Select	NP_998764.1:p.Ser726=