Canonical Allele Identifier: CA1019197457
Gene: NTSR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738024_62738025insTGCCCATCTGCCCACGTCTGC , CM000682.2:g.62738024_62738025insTGCCCATCTGCCCACGTCTGC GRCh38
NC_000020.10:g.61369376_61369377insTGCCCATCTGCCCACGTCTGC , CM000682.1:g.61369376_61369377insTGCCCATCTGCCCACGTCTGC GRCh37
NC_000020.9:g.60839821_60839822insTGCCCATCTGCCCACGTCTGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370501.4:c.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC MANE Select ENSP00000359532.3:n.715-16661_715-16660insTGCCCATCTGCCCACGTCT...
ENST00000370501.3:c.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC ENSP00000359532.3:n.715-16661_715-16660insTGCCCATCTGCCCACGTCT...
NM_002531.2:c.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC NP_002522.2:n.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC
XM_011528827.1:c.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC XP_011527129.1:n.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC
XM_011528827.2:c.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC XP_011527129.1:n.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC
NM_002531.3:c.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC MANE Select NP_002522.2:n.715-16661_715-16660insTGCCCATCTGCCCACGTCTGC