Canonical Allele Identifier: CA379922675

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262219A>G , CM000673.2:g.22262219A>G	GRCh38
NC_000011.9:g.22283765A>G , CM000673.1:g.22283765A>G	GRCh37
NC_000011.8:g.22240341A>G	NCBI36
NG_015844.1:g.74044A>G , LRG_868:g.74044A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1721A>G MANE Select	NP_998764.1:p.Tyr574Cys
ENST00000324559.9:c.1721A>G MANE Select	ENSP00000315371.9:p.Tyr574Cys
NM_001142649.1:c.1718A>G	NP_001136121.1:p.Tyr573Cys
NM_001142649.2:c.1718A>G	NP_001136121.1:p.Tyr573Cys
NM_213599.2:c.1721A>G , LRG_868t1:c.1721A>G	NP_998764.1:p.Tyr574Cys
ENST00000324559.8:c.1721A>G	ENSP00000315371.8:p.Tyr574Cys
ENST00000648804.1:n.2056A>G
ENST00000682266.1:c.1271A>G	ENSP00000507766.1:p.Tyr424Cys
ENST00000682341.1:c.1679A>G	ENSP00000508251.1:p.Tyr560Cys
ENST00000683197.1:c.1679A>G	ENSP00000507641.1:p.Tyr560Cys
ENST00000683411.1:c.1271A>G	ENSP00000508397.1:p.Tyr424Cys
ENST00000683437.1:c.1271A>G	ENSP00000508408.1:p.Tyr424Cys
ENST00000683613.1:n.2715A>G
ENST00000684663.1:c.1676A>G	ENSP00000508009.1:p.Tyr559Cys
XM_005252820.2:c.1679A>G	XP_005252877.2:p.Tyr560Cys
XM_005252820.3:c.1679A>G	XP_005252877.2:p.Tyr560Cys
XM_005252821.2:c.1676A>G	XP_005252878.2:p.Tyr559Cys
XM_005252821.3:c.1676A>G	XP_005252878.2:p.Tyr559Cys
XM_005252822.3:c.1643A>G	XP_005252879.1:p.Tyr548Cys
XM_005252822.4:c.1643A>G	XP_005252879.1:p.Tyr548Cys
XM_005252823.3:c.1640A>G	XP_005252880.1:p.Tyr547Cys
XM_011519949.1:c.1628A>G	XP_011518251.1:p.Tyr543Cys
XM_011519949.2:c.1628A>G	XP_011518251.1:p.Tyr543Cys