Canonical Allele Identifier: CA393935349

Gene: LINS1

Linked Data

• MyVariant Identifiers: chr15:g.101113912A>C (hg19) ; chr15:g.100573707A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573707A>C , CM000677.2:g.100573707A>C	GRCh38
NC_000015.9:g.101113912A>C , CM000677.1:g.101113912A>C	GRCh37
NC_000015.8:g.98931435A>C	NCBI36
NG_034076.1:g.33534T>G
NG_034076.2:g.34326T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1166T>G MANE Select	ENSP00000318423.8:p.Ile389Arg
ENST00000314742.12:c.1166T>G	ENSP00000318423.8:p.Ile389Arg
ENST00000559149.5:n.1323T>G
ENST00000560133.5:c.809T>G	ENSP00000454929.1:p.Ile270Arg
ENST00000560783.1:c.135T>G
ENST00000561308.5:c.1166T>G	ENSP00000454200.1:p.Ile389Arg
NM_001040616.2:c.1166T>G	NP_001035706.1:p.Ile389Arg
XM_005254941.1:c.1166T>G	XP_005254998.1:p.Ile389Arg
XM_005254943.1:c.1166T>G	XP_005255000.1:p.Ile389Arg
XR_243210.2:n.1269T>G
XR_429464.2:n.1269T>G
XR_931862.1:n.1269T>G
XR_931863.1:n.1269T>G
XR_931864.1:n.1269T>G
NM_001352507.1:c.419T>G	NP_001339436.1:p.Ile140Arg
NM_001352508.1:c.1121T>G	NP_001339437.1:p.Ile374Arg
NR_148017.1:n.1389T>G
NR_148018.1:n.1389T>G
NR_148019.1:n.1393T>G
XM_005254941.2:c.1166T>G	XP_005254998.1:p.Ile389Arg
XM_005254943.2:c.1166T>G	XP_005255000.1:p.Ile389Arg
XM_017022399.2:c.419T>G	XP_016877888.1:p.Ile140Arg
XM_017022400.2:c.419T>G	XP_016877889.1:p.Ile140Arg
XM_024449979.1:c.1166T>G	XP_024305747.1:p.Ile389Arg
XM_024449980.1:c.1166T>G	XP_024305748.1:p.Ile389Arg
XR_001751346.2:n.2181T>G
XR_001751347.2:n.2181T>G
XR_001751348.2:n.2181T>G
XR_002957655.1:n.2181T>G
XR_931862.3:n.2181T>G
NM_001040616.3:c.1166T>G MANE Select	NP_001035706.2:p.Ile389Arg
NM_001352507.2:c.419T>G	NP_001339436.1:p.Ile140Arg
NM_001352508.2:c.1121T>G	NP_001339437.1:p.Ile374Arg
NR_148017.2:n.1333T>G
NR_148018.2:n.1333T>G
NR_148019.2:n.1337T>G