Canonical Allele Identifier: CA1174911584
Gene: NEGR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.71605553T= , CM000663.2:g.71605553T= GRCh38
NC_000001.10:g.72071236T= , CM000663.1:g.72071236T= GRCh37
NC_000001.9:g.71843824T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357731.10:c.788+5473A= MANE Select ENSP00000350364.4:n.788+5473A=
ENST00000306821.3:c.404+5473A= ENSP00000305938.3:n.404+5473A=
ENST00000357731.9:c.788+5473A= ENSP00000350364.4:n.788+5473A=
ENST00000434200.5:c.623+5473A= ENSP00000413294.2:n.623+5473A=
NM_173808.2:c.788+5473A= NP_776169.2:n.788+5473A=
XM_011541200.1:c.788+5473A= XP_011539502.1:n.788+5473A=
XM_011541200.3:c.788+5473A= XP_011539502.1:n.788+5473A=
NM_173808.3:c.788+5473A= MANE Select NP_776169.2:n.788+5473A=