Canonical Allele Identifier: CA3182873560

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22226041G= , CM000673.2:g.22226041G=	GRCh38
NC_000011.9:g.22247587G= , CM000673.1:g.22247587G=	GRCh37
NC_000011.8:g.22204163G=	NCBI36
NG_015844.1:g.37866G= , LRG_868:g.37866G=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.352G= MANE Select	NP_998764.1:p.Glu118=
ENST00000324559.9:c.352G= MANE Select	ENSP00000315371.9:p.Glu118=
NM_001142649.1:c.349G=	NP_001136121.1:p.Glu117=
NM_001142649.2:c.349G=	NP_001136121.1:p.Glu117=
NM_213599.2:c.352G= , LRG_868t1:c.352G=	NP_998764.1:p.Glu118=
ENST00000324559.8:c.352G=	ENSP00000315371.8:p.Glu118=
ENST00000648804.1:n.917G=
ENST00000682266.1:c.-99G=	ENSP00000507766.1:n.-99G=
ENST00000682341.1:c.310G=	ENSP00000508251.1:p.Glu104=
ENST00000682530.1:c.*284G=	ENSP00000506805.1:n.*284G=
ENST00000682684.1:n.731G=
ENST00000683197.1:c.310G=	ENSP00000507641.1:p.Glu104=
ENST00000683411.1:c.-99G=	ENSP00000508397.1:n.-99G=
ENST00000683437.1:c.-99G=	ENSP00000508408.1:n.-99G=
ENST00000683613.1:n.1346G=
ENST00000683834.1:n.552G=
ENST00000684663.1:c.307G=	ENSP00000508009.1:p.Glu103=
XM_005252820.2:c.310G=	XP_005252877.2:p.Glu104=
XM_005252820.3:c.310G=	XP_005252877.2:p.Glu104=
XM_005252821.2:c.307G=	XP_005252878.2:p.Glu103=
XM_005252821.3:c.307G=	XP_005252878.2:p.Glu103=
XM_005252822.3:c.274G=	XP_005252879.1:p.Glu92=
XM_005252822.4:c.274G=	XP_005252879.1:p.Glu92=
XM_005252823.3:c.271G=	XP_005252880.1:p.Glu91=
XM_011519949.1:c.259G=	XP_011518251.1:p.Glu87=
XM_011519949.2:c.259G=	XP_011518251.1:p.Glu87=