Canonical Allele Identifier: CA2263605828

Gene: NGFR NGFR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49508905C= , CM000679.2:g.49508905C=	GRCh38
NC_000017.10:g.47586267C= , CM000679.1:g.47586267C=	GRCh37
NC_000017.9:g.44941266C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000172229.8:c.569-1507C= (NGFR) MANE Select	ENSP00000172229.3:n.569-1507C=
ENST00000172229.7:c.569-1507C= (NGFR)	ENSP00000172229.3:n.569-1507C=
ENST00000504201.1:c.287-1507C= (NGFR)	ENSP00000421731.1:n.287-1507C=
NM_002507.3:c.569-1507C= (NGFR)	NP_002498.1:n.569-1507C=
NR_103773.1:n.377+2078G= (NGFR-AS1)
NM_002507.4:c.569-1507C= (NGFR) MANE Select	NP_002498.1:n.569-1507C=