Canonical Allele Identifier: CA2816968004
Gene: NTSR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738035_62738036insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT , CM000682.2:g.62738035_62738036insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT GRCh38
NC_000020.10:g.61369387_61369388insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT , CM000682.1:g.61369387_61369388insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT GRCh37
NC_000020.9:g.60839832_60839833insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370501.4:c.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT MANE Select ENSP00000359532.3:n.715-16650_715-16649insGCCCTGCAGTGCCCATCTG...
ENST00000370501.3:c.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT ENSP00000359532.3:n.715-16650_715-16649insGCCCTGCAGTGCCCATCTG...
NM_002531.2:c.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT NP_002522.2:n.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACG...
XM_011528827.1:c.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT XP_011527129.1:n.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCC...
XM_011528827.2:c.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT XP_011527129.1:n.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCC...
NM_002531.3:c.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTT MANE Select NP_002522.2:n.715-16650_715-16649insGCCCTGCAGTGCCCATCTGCCCACG...