Canonical Allele Identifier: CA393935417

Gene: LINS1

Linked Data

• MyVariant Identifiers: chr15:g.101113946C>A (hg19) ; chr15:g.100573741C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573741C>A , CM000677.2:g.100573741C>A	GRCh38
NC_000015.9:g.101113946C>A , CM000677.1:g.101113946C>A	GRCh37
NC_000015.8:g.98931469C>A	NCBI36
NG_034076.1:g.33500G>T
NG_034076.2:g.34292G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1132G>T MANE Select	ENSP00000318423.8:p.Asp378Tyr
ENST00000314742.12:c.1132G>T	ENSP00000318423.8:p.Asp378Tyr
ENST00000559149.5:n.1289G>T
ENST00000560133.5:c.775G>T	ENSP00000454929.1:p.Asp259Tyr
ENST00000560783.1:c.101G>T
ENST00000561308.5:c.1132G>T	ENSP00000454200.1:p.Asp378Tyr
NM_001040616.2:c.1132G>T	NP_001035706.1:p.Asp378Tyr
XM_005254941.1:c.1132G>T	XP_005254998.1:p.Asp378Tyr
XM_005254943.1:c.1132G>T	XP_005255000.1:p.Asp378Tyr
XR_243210.2:n.1235G>T
XR_429464.2:n.1235G>T
XR_931862.1:n.1235G>T
XR_931863.1:n.1235G>T
XR_931864.1:n.1235G>T
NM_001352507.1:c.385G>T	NP_001339436.1:p.Asp129Tyr
NM_001352508.1:c.1087G>T	NP_001339437.1:p.Asp363Tyr
NR_148017.1:n.1355G>T
NR_148018.1:n.1355G>T
NR_148019.1:n.1359G>T
XM_005254941.2:c.1132G>T	XP_005254998.1:p.Asp378Tyr
XM_005254943.2:c.1132G>T	XP_005255000.1:p.Asp378Tyr
XM_017022399.2:c.385G>T	XP_016877888.1:p.Asp129Tyr
XM_017022400.2:c.385G>T	XP_016877889.1:p.Asp129Tyr
XM_024449979.1:c.1132G>T	XP_024305747.1:p.Asp378Tyr
XM_024449980.1:c.1132G>T	XP_024305748.1:p.Asp378Tyr
XR_001751346.2:n.2147G>T
XR_001751347.2:n.2147G>T
XR_001751348.2:n.2147G>T
XR_002957655.1:n.2147G>T
XR_931862.3:n.2147G>T
NM_001040616.3:c.1132G>T MANE Select	NP_001035706.2:p.Asp378Tyr
NM_001352507.2:c.385G>T	NP_001339436.1:p.Asp129Tyr
NM_001352508.2:c.1087G>T	NP_001339437.1:p.Asp363Tyr
NR_148017.2:n.1299G>T
NR_148018.2:n.1299G>T
NR_148019.2:n.1303G>T