Canonical Allele Identifier: CA2816968002
Gene: NTSR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738025_62738026insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC , CM000682.2:g.62738025_62738026insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC GRCh38
NC_000020.10:g.61369377_61369378insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC , CM000682.1:g.61369377_61369378insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC GRCh37
NC_000020.9:g.60839822_60839823insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370501.4:c.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC MANE Select ENSP00000359532.3:n.715-16660_715-16659insAGCATCCCTTTCCCTGCAG...
ENST00000370501.3:c.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC ENSP00000359532.3:n.715-16660_715-16659insAGCATCCCTTTCCCTGCAG...
NM_002531.2:c.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC NP_002522.2:n.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCA...
XM_011528827.1:c.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC XP_011527129.1:n.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGC...
XM_011528827.2:c.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC XP_011527129.1:n.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGC...
NM_002531.3:c.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCC MANE Select NP_002522.2:n.715-16660_715-16659insAGCATCCCTTTCCCTGCAGTGCCCA...