Canonical Allele Identifier: CA2374419256
Gene: NTSR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738024G= , CM000682.2:g.62738024G= GRCh38
NC_000020.10:g.61369376G= , CM000682.1:g.61369376G= GRCh37
NC_000020.9:g.60839821G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370501.4:c.715-16661G= MANE Select ENSP00000359532.3:n.715-16661G=
ENST00000370501.3:c.715-16661G= ENSP00000359532.3:n.715-16661G=
NM_002531.2:c.715-16661G= NP_002522.2:n.715-16661G=
XM_011528827.1:c.715-16661G= XP_011527129.1:n.715-16661G=
XM_011528827.2:c.715-16661G= XP_011527129.1:n.715-16661G=
NM_002531.3:c.715-16661G= MANE Select NP_002522.2:n.715-16661G=
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