Canonical Allele Identifier: CA1957395185

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22221121_22221123delinsGAT , CM000673.2:g.22221121_22221123delinsGAT	GRCh38
NC_000011.9:g.22242667_22242669delinsGAT , CM000673.1:g.22242667_22242669delinsGAT	GRCh37
NC_000011.8:g.22199243_22199245delinsGAT	NCBI36
NG_015844.1:g.32946_32948delinsGAT , LRG_868:g.32946_32948delinsGAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.-246_-244delinsGAT	ENSP00000507766.1:n.-246_-244delinsGAT
ENST00000682341.1:c.163_165delinsGAT	ENSP00000508251.1:p.Asp55=
ENST00000682530.1:c.*137_*139delinsGAT	ENSP00000506805.1:n.*137_*139delinsGAT
ENST00000682684.1:n.584_586delinsGAT
ENST00000683197.1:c.163_165delinsGAT	ENSP00000507641.1:p.Asp55=
ENST00000683411.1:c.-246_-244delinsGAT	ENSP00000508397.1:n.-246_-244delinsGAT
ENST00000683437.1:c.-246_-244delinsGAT	ENSP00000508408.1:n.-246_-244delinsGAT
ENST00000683613.1:n.1199_1201delinsGAT
ENST00000683834.1:n.405_407delinsGAT
ENST00000683897.1:n.449_451delinsGAT
ENST00000684365.1:n.574_576delinsGAT
ENST00000684663.1:c.160_162delinsGAT	ENSP00000508009.1:p.Asp54=
ENST00000324559.9:c.205_207delinsGAT MANE Select	ENSP00000315371.9:p.Asp69=
ENST00000648804.1:n.770_772delinsGAT
ENST00000324559.8:c.205_207delinsGAT	ENSP00000315371.8:p.Asp69=
NM_001142649.1:c.202_204delinsGAT	NP_001136121.1:p.Asp68=
NM_213599.2:c.205_207delinsGAT , LRG_868t1:c.205_207delinsGAT	NP_998764.1:p.Asp69=
XM_005252820.2:c.163_165delinsGAT	XP_005252877.2:p.Asp55=
XM_005252821.2:c.160_162delinsGAT	XP_005252878.2:p.Asp54=
XM_005252822.3:c.127_129delinsGAT	XP_005252879.1:p.Asp43=
XM_005252823.3:c.124_126delinsGAT	XP_005252880.1:p.Asp42=
XM_011519949.1:c.112_114delinsGAT	XP_011518251.1:p.Asp38=
XM_005252820.3:c.163_165delinsGAT	XP_005252877.2:p.Asp55=
XM_005252821.3:c.160_162delinsGAT	XP_005252878.2:p.Asp54=
XM_005252822.4:c.127_129delinsGAT	XP_005252879.1:p.Asp43=
XM_011519949.2:c.112_114delinsGAT	XP_011518251.1:p.Asp38=
NM_001142649.2:c.202_204delinsGAT	NP_001136121.1:p.Asp68=
NM_213599.3:c.205_207delinsGAT MANE Select	NP_998764.1:p.Asp69=