Canonical Allele Identifier: CA1957413222

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250324A= , CM000673.2:g.22250324A=	GRCh38
NC_000011.9:g.22271870A= , CM000673.1:g.22271870A=	GRCh37
NC_000011.8:g.22228446A=	NCBI36
NG_015844.1:g.62149A= , LRG_868:g.62149A=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.966A= MANE Select	NP_998764.1:p.Leu322=
ENST00000324559.9:c.966A= MANE Select	ENSP00000315371.9:p.Leu322=
NM_001142649.1:c.963A=	NP_001136121.1:p.Leu321=
NM_001142649.2:c.963A=	NP_001136121.1:p.Leu321=
NM_213599.2:c.966A= , LRG_868t1:c.966A=	NP_998764.1:p.Leu322=
ENST00000324559.8:c.966A=	ENSP00000315371.8:p.Leu322=
ENST00000648804.1:n.1301A=
ENST00000682089.1:n.286A=
ENST00000682266.1:c.516A=	ENSP00000507766.1:p.Leu172=
ENST00000682341.1:c.924A=	ENSP00000508251.1:p.Leu308=
ENST00000682530.1:c.*898A=	ENSP00000506805.1:n.*898A=
ENST00000683197.1:c.924A=	ENSP00000507641.1:p.Leu308=
ENST00000683411.1:c.516A=	ENSP00000508397.1:p.Leu172=
ENST00000683437.1:c.516A=	ENSP00000508408.1:p.Leu172=
ENST00000683613.1:n.1960A=
ENST00000683834.1:n.1166A=
ENST00000684663.1:c.921A=	ENSP00000508009.1:p.Leu307=
XM_005252820.2:c.924A=	XP_005252877.2:p.Leu308=
XM_005252820.3:c.924A=	XP_005252877.2:p.Leu308=
XM_005252821.2:c.921A=	XP_005252878.2:p.Leu307=
XM_005252821.3:c.921A=	XP_005252878.2:p.Leu307=
XM_005252822.3:c.888A=	XP_005252879.1:p.Leu296=
XM_005252822.4:c.888A=	XP_005252879.1:p.Leu296=
XM_005252823.3:c.885A=	XP_005252880.1:p.Leu295=
XM_011519949.1:c.873A=	XP_011518251.1:p.Leu291=
XM_011519949.2:c.873A=	XP_011518251.1:p.Leu291=