Canonical Allele Identifier: CA2200116906

Gene: LINS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573936C= , CM000677.2:g.100573936C=	GRCh38
NC_000015.9:g.101114141C= , CM000677.1:g.101114141C=	GRCh37
NC_000015.8:g.98931664C=	NCBI36
NG_034076.1:g.33305G=
NG_034076.2:g.34097G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001040616.3:c.937G= MANE Select	NP_001035706.2:p.Glu313=
ENST00000314742.13:c.937G= MANE Select	ENSP00000318423.8:p.Glu313=
NM_001040616.2:c.937G=	NP_001035706.1:p.Glu313=
NM_001352507.1:c.190G=	NP_001339436.1:p.Glu64=
NM_001352507.2:c.190G=	NP_001339436.1:p.Glu64=
NM_001352508.1:c.892G=	NP_001339437.1:p.Glu298=
NM_001352508.2:c.892G=	NP_001339437.1:p.Glu298=
NR_148017.1:n.1160G=
NR_148017.2:n.1104G=
NR_148018.1:n.1160G=
NR_148018.2:n.1104G=
NR_148019.1:n.1164G=
NR_148019.2:n.1108G=
ENST00000314742.12:c.937G=	ENSP00000318423.8:p.Glu313=
ENST00000559149.5:n.1094G=
ENST00000560133.5:c.580G=	ENSP00000454929.1:p.Glu194=
ENST00000561308.5:c.937G=	ENSP00000454200.1:p.Glu313=
XM_005254941.1:c.937G=	XP_005254998.1:p.Glu313=
XM_005254941.2:c.937G=	XP_005254998.1:p.Glu313=
XM_005254943.1:c.937G=	XP_005255000.1:p.Glu313=
XM_005254943.2:c.937G=	XP_005255000.1:p.Glu313=
XM_017022399.2:c.190G=	XP_016877888.1:p.Glu64=
XM_017022400.2:c.190G=	XP_016877889.1:p.Glu64=
XM_024449979.1:c.937G=	XP_024305747.1:p.Glu313=
XM_024449980.1:c.937G=	XP_024305748.1:p.Glu313=
XR_001751346.2:n.1952G=
XR_001751347.2:n.1952G=
XR_001751348.2:n.1952G=
XR_002957655.1:n.1952G=
XR_243210.2:n.1040G=
XR_429464.2:n.1040G=
XR_931862.1:n.1040G=
XR_931862.3:n.1952G=
XR_931863.1:n.1040G=
XR_931864.1:n.1040G=