Canonical Allele Identifier: CA1019197582
Gene: NTSR1 HGNC NCBI

Linked Data

dbSNP Id: rs1989130531

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738035_62738036insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT , CM000682.2:g.62738035_62738036insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT GRCh38
NC_000020.10:g.61369387_61369388insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT , CM000682.1:g.61369387_61369388insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT GRCh37
NC_000020.9:g.60839832_60839833insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370501.4:c.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT MANE Select ENSP00000359532.3:n.715-16650_715-16649insCCCCTGCAGTGCCCATCTG...
ENST00000370501.3:c.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT ENSP00000359532.3:n.715-16650_715-16649insCCCCTGCAGTGCCCATCTG...
NM_002531.2:c.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT NP_002522.2:n.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACG...
XM_011528827.1:c.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT XP_011527129.1:n.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCC...
XM_011528827.2:c.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT XP_011527129.1:n.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCC...
NM_002531.3:c.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCCCGTCTGCCCGCATCCCTT MANE Select NP_002522.2:n.715-16650_715-16649insCCCCTGCAGTGCCCATCTGCCCACG...