Canonical Allele Identifier: CA473407313

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22284506C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262960C>A , CM000673.2:g.22262960C>A	GRCh38
NC_000011.9:g.22284506C>A , CM000673.1:g.22284506C>A	GRCh37
NC_000011.8:g.22241082C>A	NCBI36
NG_015844.1:g.74785C>A , LRG_868:g.74785C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1365C>A	ENSP00000507766.1:p.Gly455=
ENST00000682341.1:c.1773C>A	ENSP00000508251.1:p.Gly591=
ENST00000683197.1:c.1773C>A	ENSP00000507641.1:p.Gly591=
ENST00000683411.1:c.1365C>A	ENSP00000508397.1:p.Gly455=
ENST00000683437.1:c.1365C>A	ENSP00000508408.1:p.Gly455=
ENST00000683613.1:n.2809C>A
ENST00000684663.1:c.1770C>A	ENSP00000508009.1:p.Gly590=
ENST00000324559.9:c.1815C>A MANE Select	ENSP00000315371.9:p.Gly605=
ENST00000648804.1:n.2150C>A
ENST00000324559.8:c.1815C>A	ENSP00000315371.8:p.Gly605=
NM_001142649.1:c.1812C>A	NP_001136121.1:p.Gly604=
NM_213599.2:c.1815C>A , LRG_868t1:c.1815C>A	NP_998764.1:p.Gly605=
XM_005252820.2:c.1773C>A	XP_005252877.2:p.Gly591=
XM_005252821.2:c.1770C>A	XP_005252878.2:p.Gly590=
XM_005252822.3:c.1737C>A	XP_005252879.1:p.Gly579=
XM_005252823.3:c.1734C>A	XP_005252880.1:p.Gly578=
XM_011519949.1:c.1722C>A	XP_011518251.1:p.Gly574=
XM_005252820.3:c.1773C>A	XP_005252877.2:p.Gly591=
XM_005252821.3:c.1770C>A	XP_005252878.2:p.Gly590=
XM_005252822.4:c.1737C>A	XP_005252879.1:p.Gly579=
XM_011519949.2:c.1722C>A	XP_011518251.1:p.Gly574=
NM_001142649.2:c.1812C>A	NP_001136121.1:p.Gly604=
NM_213599.3:c.1815C>A MANE Select	NP_998764.1:p.Gly605=