Canonical Allele Identifier: CA1003032113
Gene: NEGR1 HGNC NCBI

Linked Data

dbSNP Id: rs1650050101
gnomAD v3: 1-71605494-A-G
gnomAD v4: 1-71605494-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.71605494A>G , CM000663.2:g.71605494A>G GRCh38
NC_000001.10:g.72071177A>G , CM000663.1:g.72071177A>G GRCh37
NC_000001.9:g.71843765A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357731.10:c.788+5532T>C MANE Select ENSP00000350364.4:n.788+5532T>C
ENST00000306821.3:c.404+5532T>C ENSP00000305938.3:n.404+5532T>C
ENST00000357731.9:c.788+5532T>C ENSP00000350364.4:n.788+5532T>C
ENST00000434200.5:c.623+5532T>C ENSP00000413294.2:n.623+5532T>C
NM_173808.2:c.788+5532T>C NP_776169.2:n.788+5532T>C
XM_011541200.1:c.788+5532T>C XP_011539502.1:n.788+5532T>C
XM_011541200.3:c.788+5532T>C XP_011539502.1:n.788+5532T>C
NM_173808.3:c.788+5532T>C MANE Select NP_776169.2:n.788+5532T>C
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