Canonical Allele Identifier: CA1019197652
Gene: NTSR1 HGNC NCBI

Linked Data

dbSNP Id: rs1989130347

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738025_62738026insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC , CM000682.2:g.62738025_62738026insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC GRCh38
NC_000020.10:g.61369377_61369378insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC , CM000682.1:g.61369377_61369378insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC GRCh37
NC_000020.9:g.60839822_60839823insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370501.4:c.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC MANE Select ENSP00000359532.3:n.715-16660_715-16659insATCCCTTTCCCTGCAGTGC...
ENST00000370501.3:c.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC ENSP00000359532.3:n.715-16660_715-16659insATCCCTTTCCCTGCAGTGC...
NM_002531.2:c.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC NP_002522.2:n.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCT...
XM_011528827.1:c.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC XP_011527129.1:n.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCA...
XM_011528827.2:c.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC XP_011527129.1:n.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCA...
NM_002531.3:c.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC MANE Select NP_002522.2:n.715-16660_715-16659insATCCCTTTCCCTGCAGTGCCCATCT...