Canonical Allele Identifier: CA393935477

Gene: LINS1

Linked Data

• MyVariant Identifiers: chr15:g.101113973G>T (hg19) ; chr15:g.100573768G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573768G>T , CM000677.2:g.100573768G>T	GRCh38
NC_000015.9:g.101113973G>T , CM000677.1:g.101113973G>T	GRCh37
NC_000015.8:g.98931496G>T	NCBI36
NG_034076.1:g.33473C>A
NG_034076.2:g.34265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1105C>A MANE Select	ENSP00000318423.8:p.Pro369Thr
ENST00000314742.12:c.1105C>A	ENSP00000318423.8:p.Pro369Thr
ENST00000559149.5:n.1262C>A
ENST00000560133.5:c.748C>A	ENSP00000454929.1:p.Pro250Thr
ENST00000560783.1:c.74C>A
ENST00000561308.5:c.1105C>A	ENSP00000454200.1:p.Pro369Thr
NM_001040616.2:c.1105C>A	NP_001035706.1:p.Pro369Thr
XM_005254941.1:c.1105C>A	XP_005254998.1:p.Pro369Thr
XM_005254943.1:c.1105C>A	XP_005255000.1:p.Pro369Thr
XR_243210.2:n.1208C>A
XR_429464.2:n.1208C>A
XR_931862.1:n.1208C>A
XR_931863.1:n.1208C>A
XR_931864.1:n.1208C>A
NM_001352507.1:c.358C>A	NP_001339436.1:p.Pro120Thr
NM_001352508.1:c.1060C>A	NP_001339437.1:p.Pro354Thr
NR_148017.1:n.1328C>A
NR_148018.1:n.1328C>A
NR_148019.1:n.1332C>A
XM_005254941.2:c.1105C>A	XP_005254998.1:p.Pro369Thr
XM_005254943.2:c.1105C>A	XP_005255000.1:p.Pro369Thr
XM_017022399.2:c.358C>A	XP_016877888.1:p.Pro120Thr
XM_017022400.2:c.358C>A	XP_016877889.1:p.Pro120Thr
XM_024449979.1:c.1105C>A	XP_024305747.1:p.Pro369Thr
XM_024449980.1:c.1105C>A	XP_024305748.1:p.Pro369Thr
XR_001751346.2:n.2120C>A
XR_001751347.2:n.2120C>A
XR_001751348.2:n.2120C>A
XR_002957655.1:n.2120C>A
XR_931862.3:n.2120C>A
NM_001040616.3:c.1105C>A MANE Select	NP_001035706.2:p.Pro369Thr
NM_001352507.2:c.358C>A	NP_001339436.1:p.Pro120Thr
NM_001352508.2:c.1060C>A	NP_001339437.1:p.Pro354Thr
NR_148017.2:n.1272C>A
NR_148018.2:n.1272C>A
NR_148019.2:n.1276C>A