Canonical Allele Identifier: CA1019197474
Gene: NTSR1 HGNC NCBI

Linked Data

dbSNP Id: rs1989130613

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738037_62738038insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC , CM000682.2:g.62738037_62738038insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC GRCh38
NC_000020.10:g.61369389_61369390insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC , CM000682.1:g.61369389_61369390insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC GRCh37
NC_000020.9:g.60839834_60839835insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370501.4:c.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC MANE Select ENSP00000359532.3:n.715-16648_715-16647insTCTGCAGTGCCCATCTGCC...
ENST00000370501.3:c.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC ENSP00000359532.3:n.715-16648_715-16647insTCTGCAGTGCCCATCTGCC...
NM_002531.2:c.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC NP_002522.2:n.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTC...
XM_011528827.1:c.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC XP_011527129.1:n.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCAC...
XM_011528827.2:c.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC XP_011527129.1:n.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCAC...
NM_002531.3:c.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTC MANE Select NP_002522.2:n.715-16648_715-16647insTCTGCAGTGCCCATCTGCCCACGTC...