Canonical Allele Identifier: CA473407511

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294391T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272845T>A , CM000673.2:g.22272845T>A	GRCh38
NC_000011.9:g.22294391T>A , CM000673.1:g.22294391T>A	GRCh37
NC_000011.8:g.22250967T>A	NCBI36
NG_015844.1:g.84670T>A , LRG_868:g.84670T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.108T>A
ENST00000682266.1:c.1641T>A	ENSP00000507766.1:p.Ala547=
ENST00000682341.1:c.2049T>A	ENSP00000508251.1:p.Ala683=
ENST00000683197.1:c.2049T>A	ENSP00000507641.1:p.Ala683=
ENST00000683411.1:c.1641T>A	ENSP00000508397.1:p.Ala547=
ENST00000683437.1:c.1641T>A	ENSP00000508408.1:p.Ala547=
ENST00000683613.1:n.3085T>A
ENST00000684663.1:c.2046T>A	ENSP00000508009.1:p.Ala682=
ENST00000324559.9:c.2091T>A MANE Select	ENSP00000315371.9:p.Ala697=
ENST00000648804.1:n.2426T>A
ENST00000324559.8:c.2091T>A	ENSP00000315371.8:p.Ala697=
ENST00000532043.1:n.108T>A
NM_001142649.1:c.2088T>A	NP_001136121.1:p.Ala696=
NM_213599.2:c.2091T>A , LRG_868t1:c.2091T>A	NP_998764.1:p.Ala697=
XM_005252820.2:c.2049T>A	XP_005252877.2:p.Ala683=
XM_005252821.2:c.2046T>A	XP_005252878.2:p.Ala682=
XM_005252822.3:c.2013T>A	XP_005252879.1:p.Ala671=
XM_005252823.3:c.2010T>A	XP_005252880.1:p.Ala670=
XM_011519949.1:c.1998T>A	XP_011518251.1:p.Ala666=
XM_005252820.3:c.2049T>A	XP_005252877.2:p.Ala683=
XM_005252821.3:c.2046T>A	XP_005252878.2:p.Ala682=
XM_005252822.4:c.2013T>A	XP_005252879.1:p.Ala671=
XM_011519949.2:c.1998T>A	XP_011518251.1:p.Ala666=
NM_001142649.2:c.2088T>A	NP_001136121.1:p.Ala696=
NM_213599.3:c.2091T>A MANE Select	NP_998764.1:p.Ala697=