Canonical Allele Identifier: CA7759537
Gene: LINS1 HGNC NCBI

Linked Data

dbSNP Id: rs751128055

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100573791A>C , CM000677.2:g.100573791A>C GRCh38
NC_000015.9:g.101113996A>C , CM000677.1:g.101113996A>C GRCh37
NC_000015.8:g.98931519A>C NCBI36
NG_034076.1:g.33450T>G
NG_034076.2:g.34242T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000314742.13:c.1082T>G MANE Select ENSP00000318423.8:p.Phe361Cys
ENST00000314742.12:c.1082T>G ENSP00000318423.8:p.Phe361Cys
ENST00000559149.5:n.1239T>G
ENST00000560133.5:c.725T>G ENSP00000454929.1:p.Phe242Cys
ENST00000560783.1:c.51T>G
ENST00000561308.5:c.1082T>G ENSP00000454200.1:p.Phe361Cys
NM_001040616.2:c.1082T>G NP_001035706.1:p.Phe361Cys
XM_005254941.1:c.1082T>G XP_005254998.1:p.Phe361Cys
XM_005254943.1:c.1082T>G XP_005255000.1:p.Phe361Cys
XR_243210.2:n.1185T>G
XR_429464.2:n.1185T>G
XR_931862.1:n.1185T>G
XR_931863.1:n.1185T>G
XR_931864.1:n.1185T>G
NM_001352507.1:c.335T>G NP_001339436.1:p.Phe112Cys
NM_001352508.1:c.1037T>G NP_001339437.1:p.Phe346Cys
NR_148017.1:n.1305T>G
NR_148018.1:n.1305T>G
NR_148019.1:n.1309T>G
XM_005254941.2:c.1082T>G XP_005254998.1:p.Phe361Cys
XM_005254943.2:c.1082T>G XP_005255000.1:p.Phe361Cys
XM_017022399.2:c.335T>G XP_016877888.1:p.Phe112Cys
XM_017022400.2:c.335T>G XP_016877889.1:p.Phe112Cys
XM_024449979.1:c.1082T>G XP_024305747.1:p.Phe361Cys
XM_024449980.1:c.1082T>G XP_024305748.1:p.Phe361Cys
XR_001751346.2:n.2097T>G
XR_001751347.2:n.2097T>G
XR_001751348.2:n.2097T>G
XR_002957655.1:n.2097T>G
XR_931862.3:n.2097T>G
NM_001040616.3:c.1082T>G MANE Select NP_001035706.2:p.Phe361Cys
NM_001352507.2:c.335T>G NP_001339436.1:p.Phe112Cys
NM_001352508.2:c.1037T>G NP_001339437.1:p.Phe346Cys
NR_148017.2:n.1249T>G
NR_148018.2:n.1249T>G
NR_148019.2:n.1253T>G