Canonical Allele Identifier: CA1019197261
Gene: NTSR1 HGNC NCBI

Linked Data

dbSNP Id: rs1989130291
gnomAD v3: 20-62738023-A-ACCC
gnomAD v4: 20-62738023-A-ACCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738023_62738024insCCC , CM000682.2:g.62738023_62738024insCCC GRCh38
NC_000020.10:g.61369375_61369376insCCC , CM000682.1:g.61369375_61369376insCCC GRCh37
NC_000020.9:g.60839820_60839821insCCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370501.4:c.715-16662_715-16661insCCC MANE Select ENSP00000359532.3:n.715-16662_715-16661insCCC
ENST00000370501.3:c.715-16662_715-16661insCCC ENSP00000359532.3:n.715-16662_715-16661insCCC
NM_002531.2:c.715-16662_715-16661insCCC NP_002522.2:n.715-16662_715-16661insCCC
XM_011528827.1:c.715-16662_715-16661insCCC XP_011527129.1:n.715-16662_715-16661insCCC
XM_011528827.2:c.715-16662_715-16661insCCC XP_011527129.1:n.715-16662_715-16661insCCC
NM_002531.3:c.715-16662_715-16661insCCC MANE Select NP_002522.2:n.715-16662_715-16661insCCC
Search 100 bp 5'
Search 100 bp 3'