Canonical Allele Identifier: CA2521883681

Gene: NEGR1 NEGR1-IT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.71808706C>T , CM000663.2:g.71808706C>T	GRCh38
NC_000001.10:g.72274389C>T , CM000663.1:g.72274389C>T	GRCh37
NC_000001.9:g.72046977C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357731.10:c.410-32409G>A (NEGR1) MANE Select	ENSP00000350364.4:n.410-32409G>A
ENST00000306821.3:c.26-32409G>A (NEGR1)	ENSP00000305938.3:n.26-32409G>A
ENST00000357731.9:c.410-32409G>A (NEGR1)	ENSP00000350364.4:n.410-32409G>A
ENST00000434200.5:c.245-32409G>A (NEGR1)	ENSP00000413294.2:n.245-32409G>A
ENST00000467479.1:n.407-32409G>A (NEGR1)
NM_173808.2:c.410-32409G>A (NEGR1)	NP_776169.2:n.410-32409G>A
NR_046218.1:n.34-10436G>A (NEGR1-IT1)
XM_011541200.1:c.410-32409G>A (NEGR1)	XP_011539502.1:n.410-32409G>A
XM_011541201.1:c.410-32409G>A (NEGR1)	XP_011539503.1:n.410-32409G>A
XM_011541200.3:c.410-32409G>A (NEGR1)	XP_011539502.1:n.410-32409G>A
XM_011541201.3:c.410-32409G>A (NEGR1)	XP_011539503.1:n.410-32409G>A
XM_017000961.2:c.410-32409G>A (NEGR1)	XP_016856450.1:n.410-32409G>A
NM_173808.3:c.410-32409G>A (NEGR1) MANE Select	NP_776169.2:n.410-32409G>A