Canonical Allele Identifier: CA473407385

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22291864T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22270318T>A , CM000673.2:g.22270318T>A	GRCh38
NC_000011.9:g.22291864T>A , CM000673.1:g.22291864T>A	GRCh37
NC_000011.8:g.22248440T>A	NCBI36
NG_015844.1:g.82143T>A , LRG_868:g.82143T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1455T>A	ENSP00000507766.1:p.Ala485=
ENST00000682341.1:c.1863T>A	ENSP00000508251.1:p.Ala621=
ENST00000683197.1:c.1863T>A	ENSP00000507641.1:p.Ala621=
ENST00000683411.1:c.1455T>A	ENSP00000508397.1:p.Ala485=
ENST00000683437.1:c.1455T>A	ENSP00000508408.1:p.Ala485=
ENST00000683613.1:n.2899T>A
ENST00000684663.1:c.1860T>A	ENSP00000508009.1:p.Ala620=
ENST00000324559.9:c.1905T>A MANE Select	ENSP00000315371.9:p.Ala635=
ENST00000648804.1:n.2240T>A
ENST00000324559.8:c.1905T>A	ENSP00000315371.8:p.Ala635=
NM_001142649.1:c.1902T>A	NP_001136121.1:p.Ala634=
NM_213599.2:c.1905T>A , LRG_868t1:c.1905T>A	NP_998764.1:p.Ala635=
XM_005252820.2:c.1863T>A	XP_005252877.2:p.Ala621=
XM_005252821.2:c.1860T>A	XP_005252878.2:p.Ala620=
XM_005252822.3:c.1827T>A	XP_005252879.1:p.Ala609=
XM_005252823.3:c.1824T>A	XP_005252880.1:p.Ala608=
XM_011519949.1:c.1812T>A	XP_011518251.1:p.Ala604=
XM_005252820.3:c.1863T>A	XP_005252877.2:p.Ala621=
XM_005252821.3:c.1860T>A	XP_005252878.2:p.Ala620=
XM_005252822.4:c.1827T>A	XP_005252879.1:p.Ala609=
XM_011519949.2:c.1812T>A	XP_011518251.1:p.Ala604=
NM_001142649.2:c.1902T>A	NP_001136121.1:p.Ala634=
NM_213599.3:c.1905T>A MANE Select	NP_998764.1:p.Ala635=