Canonical Allele Identifier: CA2200116623

Gene: LINS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573743G= , CM000677.2:g.100573743G=	GRCh38
NC_000015.9:g.101113948G= , CM000677.1:g.101113948G=	GRCh37
NC_000015.8:g.98931471G=	NCBI36
NG_034076.1:g.33498C=
NG_034076.2:g.34290C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1130C= MANE Select	ENSP00000318423.8:p.Pro377=
ENST00000314742.12:c.1130C=	ENSP00000318423.8:p.Pro377=
ENST00000559149.5:n.1287C=
ENST00000560133.5:c.773C=	ENSP00000454929.1:p.Pro258=
ENST00000560783.1:c.99C=
ENST00000561308.5:c.1130C=	ENSP00000454200.1:p.Pro377=
NM_001040616.2:c.1130C=	NP_001035706.1:p.Pro377=
XM_005254941.1:c.1130C=	XP_005254998.1:p.Pro377=
XM_005254943.1:c.1130C=	XP_005255000.1:p.Pro377=
XR_243210.2:n.1233C=
XR_429464.2:n.1233C=
XR_931862.1:n.1233C=
XR_931863.1:n.1233C=
XR_931864.1:n.1233C=
NM_001352507.1:c.383C=	NP_001339436.1:p.Pro128=
NM_001352508.1:c.1085C=	NP_001339437.1:p.Pro362=
NR_148017.1:n.1353C=
NR_148018.1:n.1353C=
NR_148019.1:n.1357C=
XM_005254941.2:c.1130C=	XP_005254998.1:p.Pro377=
XM_005254943.2:c.1130C=	XP_005255000.1:p.Pro377=
XM_017022399.2:c.383C=	XP_016877888.1:p.Pro128=
XM_017022400.2:c.383C=	XP_016877889.1:p.Pro128=
XM_024449979.1:c.1130C=	XP_024305747.1:p.Pro377=
XM_024449980.1:c.1130C=	XP_024305748.1:p.Pro377=
XR_001751346.2:n.2145C=
XR_001751347.2:n.2145C=
XR_001751348.2:n.2145C=
XR_002957655.1:n.2145C=
XR_931862.3:n.2145C=
NM_001040616.3:c.1130C= MANE Select	NP_001035706.2:p.Pro377=
NM_001352507.2:c.383C=	NP_001339436.1:p.Pro128=
NM_001352508.2:c.1085C=	NP_001339437.1:p.Pro362=
NR_148017.2:n.1297C=
NR_148018.2:n.1297C=
NR_148019.2:n.1301C=