Canonical Allele Identifier: CA2200116500

Gene: LINS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573668G= , CM000677.2:g.100573668G=	GRCh38
NC_000015.9:g.101113873G= , CM000677.1:g.101113873G=	GRCh37
NC_000015.8:g.98931396G=	NCBI36
NG_034076.1:g.33573C=
NG_034076.2:g.34365C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1205C= MANE Select	ENSP00000318423.8:p.Ser402=
ENST00000314742.12:c.1205C=	ENSP00000318423.8:p.Ser402=
ENST00000559149.5:n.1362C=
ENST00000560133.5:c.848C=	ENSP00000454929.1:p.Ser283=
ENST00000560783.1:c.174C=
ENST00000561308.5:c.1205C=	ENSP00000454200.1:p.Ser402=
NM_001040616.2:c.1205C=	NP_001035706.1:p.Ser402=
XM_005254941.1:c.1205C=	XP_005254998.1:p.Ser402=
XM_005254943.1:c.1205C=	XP_005255000.1:p.Ser402=
XR_243210.2:n.1308C=
XR_429464.2:n.1308C=
XR_931862.1:n.1308C=
XR_931863.1:n.1308C=
XR_931864.1:n.1308C=
NM_001352507.1:c.458C=	NP_001339436.1:p.Ser153=
NM_001352508.1:c.1160C=	NP_001339437.1:p.Ser387=
NR_148017.1:n.1428C=
NR_148018.1:n.1428C=
NR_148019.1:n.1432C=
XM_005254941.2:c.1205C=	XP_005254998.1:p.Ser402=
XM_005254943.2:c.1205C=	XP_005255000.1:p.Ser402=
XM_017022399.2:c.458C=	XP_016877888.1:p.Ser153=
XM_017022400.2:c.458C=	XP_016877889.1:p.Ser153=
XM_024449979.1:c.1205C=	XP_024305747.1:p.Ser402=
XM_024449980.1:c.1205C=	XP_024305748.1:p.Ser402=
XR_001751346.2:n.2220C=
XR_001751347.2:n.2220C=
XR_001751348.2:n.2220C=
XR_002957655.1:n.2220C=
XR_931862.3:n.2220C=
NM_001040616.3:c.1205C= MANE Select	NP_001035706.2:p.Ser402=
NM_001352507.2:c.458C=	NP_001339436.1:p.Ser153=
NM_001352508.2:c.1160C=	NP_001339437.1:p.Ser387=
NR_148017.2:n.1372C=
NR_148018.2:n.1372C=
NR_148019.2:n.1376C=