Canonical Allele Identifier: CA1144107301

Gene: NGF NGF-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286802A= , CM000663.2:g.115286802A=	GRCh38
NC_000001.10:g.115829423A= , CM000663.1:g.115829423A=	GRCh37
NC_000001.9:g.115630946A=	NCBI36
NG_007944.1:g.56435T= , LRG_260:g.56435T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.-7T= (NGF) MANE Select	ENSP00000358525.2:n.-7T=
ENST00000675637.2:c.-7T= (NGF)	ENSP00000502831.1:n.-7T=
ENST00000676038.2:c.-7T= (NGF)	ENSP00000502380.1:n.-7T=
ENST00000679806.1:c.-7T= (NGF)	ENSP00000506492.1:n.-7T=
ENST00000680116.1:c.-7T= (NGF)	ENSP00000505694.1:n.-7T=
ENST00000680540.1:c.-7T= (NGF)	ENSP00000506569.1:n.-7T=
ENST00000680752.1:c.-7T= (NGF)	ENSP00000505558.1:n.-7T=
ENST00000681124.1:c.-420-58T= (NGF)	ENSP00000506364.1:n.-420-58T=
ENST00000369512.2:c.-7T= (NGF)	ENSP00000358525.2:n.-7T=
NM_002506.2:c.-7T= , LRG_260t1:c.-7T= (NGF)	NP_002497.2:n.-7T=
XM_006710663.2:c.-7T= (NGF)	XP_006710726.1:n.-7T=
XM_006710665.2:c.-7T= (NGF)	XP_006710728.1:n.-7T=
XM_011541518.1:c.159T= (NGF)	XP_011539820.1:p.His53=
NR_157569.1:n.207+3562A= (NGF-AS1)
XM_006710663.3:c.-7T= (NGF)	XP_006710726.1:n.-7T=
XM_011541518.2:c.159T= (NGF)	XP_011539820.1:p.His53=
NM_002506.3:c.-7T= (NGF) MANE Select	NP_002497.2:n.-7T=