Canonical Allele Identifier: CA2200116697

Gene: LINS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573790A= , CM000677.2:g.100573790A=	GRCh38
NC_000015.9:g.101113995A= , CM000677.1:g.101113995A=	GRCh37
NC_000015.8:g.98931518A=	NCBI36
NG_034076.1:g.33451T=
NG_034076.2:g.34243T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1083T= MANE Select	ENSP00000318423.8:p.Phe361=
ENST00000314742.12:c.1083T=	ENSP00000318423.8:p.Phe361=
ENST00000559149.5:n.1240T=
ENST00000560133.5:c.726T=	ENSP00000454929.1:p.Phe242=
ENST00000560783.1:c.52T=
ENST00000561308.5:c.1083T=	ENSP00000454200.1:p.Phe361=
NM_001040616.2:c.1083T=	NP_001035706.1:p.Phe361=
XM_005254941.1:c.1083T=	XP_005254998.1:p.Phe361=
XM_005254943.1:c.1083T=	XP_005255000.1:p.Phe361=
XR_243210.2:n.1186T=
XR_429464.2:n.1186T=
XR_931862.1:n.1186T=
XR_931863.1:n.1186T=
XR_931864.1:n.1186T=
NM_001352507.1:c.336T=	NP_001339436.1:p.Phe112=
NM_001352508.1:c.1038T=	NP_001339437.1:p.Phe346=
NR_148017.1:n.1306T=
NR_148018.1:n.1306T=
NR_148019.1:n.1310T=
XM_005254941.2:c.1083T=	XP_005254998.1:p.Phe361=
XM_005254943.2:c.1083T=	XP_005255000.1:p.Phe361=
XM_017022399.2:c.336T=	XP_016877888.1:p.Phe112=
XM_017022400.2:c.336T=	XP_016877889.1:p.Phe112=
XM_024449979.1:c.1083T=	XP_024305747.1:p.Phe361=
XM_024449980.1:c.1083T=	XP_024305748.1:p.Phe361=
XR_001751346.2:n.2098T=
XR_001751347.2:n.2098T=
XR_001751348.2:n.2098T=
XR_002957655.1:n.2098T=
XR_931862.3:n.2098T=
NM_001040616.3:c.1083T= MANE Select	NP_001035706.2:p.Phe361=
NM_001352507.2:c.336T=	NP_001339436.1:p.Phe112=
NM_001352508.2:c.1038T=	NP_001339437.1:p.Phe346=
NR_148017.2:n.1250T=
NR_148018.2:n.1250T=
NR_148019.2:n.1254T=