Canonical Allele Identifier: CA10779598

Gene: NGF NGF-AS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115300189A>T , CM000663.2:g.115300189A>T	GRCh38
NC_000001.10:g.115842810A>T , CM000663.1:g.115842810A>T	GRCh37
NC_000001.9:g.115644333A>T	NCBI36
NG_007944.1:g.43048T>A , LRG_260:g.43048T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.-136-6439T>A (NGF) MANE Select	ENSP00000358525.2:n.-136-6439T>A
ENST00000675637.2:c.-12-13382T>A (NGF)	ENSP00000502831.1:n.-12-13382T>A
ENST00000676038.2:c.-137+208T>A (NGF)	ENSP00000502380.1:n.-137+208T>A
ENST00000679806.1:c.-136-6439T>A (NGF)	ENSP00000506492.1:n.-136-6439T>A
ENST00000680116.1:c.-606-6439T>A (NGF)	ENSP00000505694.1:n.-606-6439T>A
ENST00000680752.1:c.-136-6439T>A (NGF)	ENSP00000505558.1:n.-136-6439T>A
ENST00000681124.1:c.-544-6439T>A (NGF)	ENSP00000506364.1:n.-544-6439T>A
ENST00000369512.2:c.-136-6439T>A (NGF)	ENSP00000358525.2:n.-136-6439T>A
NM_002506.2:c.-136-6439T>A , LRG_260t1:c.-136-6439T>A (NGF)	NP_002497.2:n.-136-6439T>A
XM_006710663.2:c.-12-13382T>A (NGF)	XP_006710726.1:n.-12-13382T>A
XM_006710665.2:c.-136-6439T>A (NGF)	XP_006710728.1:n.-136-6439T>A
XM_011541518.1:c.29+208T>A (NGF)	XP_011539820.1:n.29+208T>A
NR_157569.1:n.207+16949A>T (NGF-AS1)
XM_006710663.3:c.-12-13382T>A (NGF)	XP_006710726.1:n.-12-13382T>A
XM_011541518.2:c.29+208T>A (NGF)	XP_011539820.1:n.29+208T>A
NM_002506.3:c.-136-6439T>A (NGF) MANE Select	NP_002497.2:n.-136-6439T>A