Canonical Allele Identifier: CA1175002597

Gene: NEGR1 NEGR1-IT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.71808726T= , CM000663.2:g.71808726T=	GRCh38
NC_000001.10:g.72274409T= , CM000663.1:g.72274409T=	GRCh37
NC_000001.9:g.72046997T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357731.10:c.410-32429A= (NEGR1) MANE Select	ENSP00000350364.4:n.410-32429A=
ENST00000306821.3:c.26-32429A= (NEGR1)	ENSP00000305938.3:n.26-32429A=
ENST00000357731.9:c.410-32429A= (NEGR1)	ENSP00000350364.4:n.410-32429A=
ENST00000434200.5:c.245-32429A= (NEGR1)	ENSP00000413294.2:n.245-32429A=
ENST00000467479.1:n.407-32429A= (NEGR1)
NM_173808.2:c.410-32429A= (NEGR1)	NP_776169.2:n.410-32429A=
NR_046218.1:n.34-10456A= (NEGR1-IT1)
XM_011541200.1:c.410-32429A= (NEGR1)	XP_011539502.1:n.410-32429A=
XM_011541201.1:c.410-32429A= (NEGR1)	XP_011539503.1:n.410-32429A=
XM_011541200.3:c.410-32429A= (NEGR1)	XP_011539502.1:n.410-32429A=
XM_011541201.3:c.410-32429A= (NEGR1)	XP_011539503.1:n.410-32429A=
XM_017000961.2:c.410-32429A= (NEGR1)	XP_016856450.1:n.410-32429A=
NM_173808.3:c.410-32429A= (NEGR1) MANE Select	NP_776169.2:n.410-32429A=