Canonical Allele Identifier: CA393935510

Gene: LINS1

Linked Data

• dbSNP Id: rs1167328046
• MyVariant Identifiers: chr15:g.101113990C>A (hg19) ; chr15:g.100573785C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573785C>A , CM000677.2:g.100573785C>A	GRCh38
NC_000015.9:g.101113990C>A , CM000677.1:g.101113990C>A	GRCh37
NC_000015.8:g.98931513C>A	NCBI36
NG_034076.1:g.33456G>T
NG_034076.2:g.34248G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1088G>T MANE Select	ENSP00000318423.8:p.Gly363Val
ENST00000314742.12:c.1088G>T	ENSP00000318423.8:p.Gly363Val
ENST00000559149.5:n.1245G>T
ENST00000560133.5:c.731G>T	ENSP00000454929.1:p.Gly244Val
ENST00000560783.1:c.57G>T
ENST00000561308.5:c.1088G>T	ENSP00000454200.1:p.Gly363Val
NM_001040616.2:c.1088G>T	NP_001035706.1:p.Gly363Val
XM_005254941.1:c.1088G>T	XP_005254998.1:p.Gly363Val
XM_005254943.1:c.1088G>T	XP_005255000.1:p.Gly363Val
XR_243210.2:n.1191G>T
XR_429464.2:n.1191G>T
XR_931862.1:n.1191G>T
XR_931863.1:n.1191G>T
XR_931864.1:n.1191G>T
NM_001352507.1:c.341G>T	NP_001339436.1:p.Gly114Val
NM_001352508.1:c.1043G>T	NP_001339437.1:p.Gly348Val
NR_148017.1:n.1311G>T
NR_148018.1:n.1311G>T
NR_148019.1:n.1315G>T
XM_005254941.2:c.1088G>T	XP_005254998.1:p.Gly363Val
XM_005254943.2:c.1088G>T	XP_005255000.1:p.Gly363Val
XM_017022399.2:c.341G>T	XP_016877888.1:p.Gly114Val
XM_017022400.2:c.341G>T	XP_016877889.1:p.Gly114Val
XM_024449979.1:c.1088G>T	XP_024305747.1:p.Gly363Val
XM_024449980.1:c.1088G>T	XP_024305748.1:p.Gly363Val
XR_001751346.2:n.2103G>T
XR_001751347.2:n.2103G>T
XR_001751348.2:n.2103G>T
XR_002957655.1:n.2103G>T
XR_931862.3:n.2103G>T
NM_001040616.3:c.1088G>T MANE Select	NP_001035706.2:p.Gly363Val
NM_001352507.2:c.341G>T	NP_001339436.1:p.Gly114Val
NM_001352508.2:c.1043G>T	NP_001339437.1:p.Gly348Val
NR_148017.2:n.1255G>T
NR_148018.2:n.1255G>T
NR_148019.2:n.1259G>T