Canonical Allele Identifier: CA317319582

Gene: NTSR1

Linked Data

• dbSNP Id: rs1555811670
• MyVariant Identifiers: chr20:g.61369376_61369377insCCCACGTCTGC (hg19) ; chr20:g.62738024_62738025insCCCACGTCTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62738026_62738027insCACGTCTGCCC , CM000682.2:g.62738026_62738027insCACGTCTGCCC	GRCh38
NC_000020.10:g.61369378_61369379insCACGTCTGCCC , CM000682.1:g.61369378_61369379insCACGTCTGCCC	GRCh37
NC_000020.9:g.60839823_60839824insCACGTCTGCCC	NCBI36

Transcript Alleles

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