Canonical Allele Identifier: CA1019197648

Gene: NTSR1

Linked Data

• gnomAD v3: 20-62738024-G-GCCCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGC
• gnomAD v4: 20-62738024-G-GCCCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62738026_62738027insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC , CM000682.2:g.62738026_62738027insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC	GRCh38
NC_000020.10:g.61369378_61369379insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC , CM000682.1:g.61369378_61369379insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC	GRCh37
NC_000020.9:g.60839823_60839824insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000370501.4:c.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC MANE Select	ENSP00000359532.3:n.715-16659_715-16658insCCATCCCTTTCCCTGCAGT...
ENST00000370501.3:c.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC	ENSP00000359532.3:n.715-16659_715-16658insCCATCCCTTTCCCTGCAGT...
NM_002531.2:c.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC	NP_002522.2:n.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCAT...
XM_011528827.1:c.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC	XP_011527129.1:n.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCC...
XM_011528827.2:c.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC	XP_011527129.1:n.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCC...
NM_002531.3:c.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCATCTGCCCACGTCTGCCC MANE Select	NP_002522.2:n.715-16659_715-16658insCCATCCCTTTCCCTGCAGTGCCCAT...