Canonical Allele Identifier: CA2374419254
Gene: NTSR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738022C= , CM000682.2:g.62738022C= GRCh38
NC_000020.10:g.61369374C= , CM000682.1:g.61369374C= GRCh37
NC_000020.9:g.60839819C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370501.4:c.715-16663C= MANE Select ENSP00000359532.3:n.715-16663C=
ENST00000370501.3:c.715-16663C= ENSP00000359532.3:n.715-16663C=
NM_002531.2:c.715-16663C= NP_002522.2:n.715-16663C=
XM_011528827.1:c.715-16663C= XP_011527129.1:n.715-16663C=
XM_011528827.2:c.715-16663C= XP_011527129.1:n.715-16663C=
NM_002531.3:c.715-16663C= MANE Select NP_002522.2:n.715-16663C=