Canonical Allele Identifier: CA1957418765

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259661C= , CM000673.2:g.22259661C=	GRCh38
NC_000011.9:g.22281207C= , CM000673.1:g.22281207C=	GRCh37
NC_000011.8:g.22237783C=	NCBI36
NG_015844.1:g.71486C= , LRG_868:g.71486C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1100C=	ENSP00000507766.1:p.Thr367=
ENST00000682341.1:c.1508C=	ENSP00000508251.1:p.Thr503=
ENST00000683197.1:c.1508C=	ENSP00000507641.1:p.Thr503=
ENST00000683411.1:c.1100C=	ENSP00000508397.1:p.Thr367=
ENST00000683437.1:c.1100C=	ENSP00000508408.1:p.Thr367=
ENST00000683613.1:n.2544C=
ENST00000684663.1:c.1505C=	ENSP00000508009.1:p.Thr502=
ENST00000324559.9:c.1550C= MANE Select	ENSP00000315371.9:p.Thr517=
ENST00000648804.1:n.1885C=
ENST00000324559.8:c.1550C=	ENSP00000315371.8:p.Thr517=
NM_001142649.1:c.1547C=	NP_001136121.1:p.Thr516=
NM_213599.2:c.1550C= , LRG_868t1:c.1550C=	NP_998764.1:p.Thr517=
XM_005252820.2:c.1508C=	XP_005252877.2:p.Thr503=
XM_005252821.2:c.1505C=	XP_005252878.2:p.Thr502=
XM_005252822.3:c.1472C=	XP_005252879.1:p.Thr491=
XM_005252823.3:c.1469C=	XP_005252880.1:p.Thr490=
XM_011519949.1:c.1457C=	XP_011518251.1:p.Thr486=
XM_005252820.3:c.1508C=	XP_005252877.2:p.Thr503=
XM_005252821.3:c.1505C=	XP_005252878.2:p.Thr502=
XM_005252822.4:c.1472C=	XP_005252879.1:p.Thr491=
XM_011519949.2:c.1457C=	XP_011518251.1:p.Thr486=
NM_001142649.2:c.1547C=	NP_001136121.1:p.Thr516=
NM_213599.3:c.1550C= MANE Select	NP_998764.1:p.Thr517=