Canonical Allele Identifier: CA1174911583
Gene: NEGR1 HGNC NCBI

Linked Data

dbSNP Id: rs1650050962
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.71605549T>C , CM000663.2:g.71605549T>C GRCh38
NC_000001.10:g.72071232T>C , CM000663.1:g.72071232T>C GRCh37
NC_000001.9:g.71843820T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357731.10:c.788+5477A>G MANE Select ENSP00000350364.4:n.788+5477A>G
ENST00000306821.3:c.404+5477A>G ENSP00000305938.3:n.404+5477A>G
ENST00000357731.9:c.788+5477A>G ENSP00000350364.4:n.788+5477A>G
ENST00000434200.5:c.623+5477A>G ENSP00000413294.2:n.623+5477A>G
NM_173808.2:c.788+5477A>G NP_776169.2:n.788+5477A>G
XM_011541200.1:c.788+5477A>G XP_011539502.1:n.788+5477A>G
XM_011541200.3:c.788+5477A>G XP_011539502.1:n.788+5477A>G
NM_173808.3:c.788+5477A>G MANE Select NP_776169.2:n.788+5477A>G
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