Canonical Allele Identifier: CA1019197555
Gene: NTSR1 HGNC NCBI

Linked Data

dbSNP Id: rs1989130662

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738039_62738040insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC , CM000682.2:g.62738039_62738040insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC GRCh38
NC_000020.10:g.61369391_61369392insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC , CM000682.1:g.61369391_61369392insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC GRCh37
NC_000020.9:g.60839836_60839837insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370501.4:c.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC MANE Select ENSP00000359532.3:n.715-16646_715-16645insAGCAGTGCCCATCTGCCCA...
ENST00000370501.3:c.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC ENSP00000359532.3:n.715-16646_715-16645insAGCAGTGCCCATCTGCCCA...
NM_002531.2:c.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC NP_002522.2:n.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTG...
XM_011528827.1:c.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC XP_011527129.1:n.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGT...
XM_011528827.2:c.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC XP_011527129.1:n.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGT...
NM_002531.3:c.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCCGCATCCCTTTCCC MANE Select NP_002522.2:n.715-16646_715-16645insAGCAGTGCCCATCTGCCCACGTCTG...