Canonical Allele Identifier: CA492684232

Gene: LINS1

Linked Data

• MyVariant Identifiers: chr15:g.101113932A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573727A>C , CM000677.2:g.100573727A>C	GRCh38
NC_000015.9:g.101113932A>C , CM000677.1:g.101113932A>C	GRCh37
NC_000015.8:g.98931455A>C	NCBI36
NG_034076.1:g.33514T>G
NG_034076.2:g.34306T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1146T>G MANE Select	ENSP00000318423.8:p.Leu382=
ENST00000314742.12:c.1146T>G	ENSP00000318423.8:p.Leu382=
ENST00000559149.5:n.1303T>G
ENST00000560133.5:c.789T>G	ENSP00000454929.1:p.Leu263=
ENST00000560783.1:c.115T>G
ENST00000561308.5:c.1146T>G	ENSP00000454200.1:p.Leu382=
NM_001040616.2:c.1146T>G	NP_001035706.1:p.Leu382=
XM_005254941.1:c.1146T>G	XP_005254998.1:p.Leu382=
XM_005254943.1:c.1146T>G	XP_005255000.1:p.Leu382=
XR_243210.2:n.1249T>G
XR_429464.2:n.1249T>G
XR_931862.1:n.1249T>G
XR_931863.1:n.1249T>G
XR_931864.1:n.1249T>G
NM_001352507.1:c.399T>G	NP_001339436.1:p.Leu133=
NM_001352508.1:c.1101T>G	NP_001339437.1:p.Leu367=
NR_148017.1:n.1369T>G
NR_148018.1:n.1369T>G
NR_148019.1:n.1373T>G
XM_005254941.2:c.1146T>G	XP_005254998.1:p.Leu382=
XM_005254943.2:c.1146T>G	XP_005255000.1:p.Leu382=
XM_017022399.2:c.399T>G	XP_016877888.1:p.Leu133=
XM_017022400.2:c.399T>G	XP_016877889.1:p.Leu133=
XM_024449979.1:c.1146T>G	XP_024305747.1:p.Leu382=
XM_024449980.1:c.1146T>G	XP_024305748.1:p.Leu382=
XR_001751346.2:n.2161T>G
XR_001751347.2:n.2161T>G
XR_001751348.2:n.2161T>G
XR_002957655.1:n.2161T>G
XR_931862.3:n.2161T>G
NM_001040616.3:c.1146T>G MANE Select	NP_001035706.2:p.Leu382=
NM_001352507.2:c.399T>G	NP_001339436.1:p.Leu133=
NM_001352508.2:c.1101T>G	NP_001339437.1:p.Leu367=
NR_148017.2:n.1313T>G
NR_148018.2:n.1313T>G
NR_148019.2:n.1317T>G