Canonical Allele Identifier: CA29771920

Gene: NGF NGF-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115293482G>T , CM000663.2:g.115293482G>T	GRCh38
NC_000001.10:g.115836103G>T , CM000663.1:g.115836103G>T	GRCh37
NC_000001.9:g.115637626G>T	NCBI36
NG_007944.1:g.49755C>A , LRG_260:g.49755C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.-13+145C>A (NGF) MANE Select	ENSP00000358525.2:n.-13+145C>A
ENST00000675637.2:c.-12-6675C>A (NGF)	ENSP00000502831.1:n.-12-6675C>A
ENST00000676038.2:c.-13+145C>A (NGF)	ENSP00000502380.1:n.-13+145C>A
ENST00000679806.1:c.-13+145C>A (NGF)	ENSP00000506492.1:n.-13+145C>A
ENST00000680116.1:c.-483+145C>A (NGF)	ENSP00000505694.1:n.-483+145C>A
ENST00000680752.1:c.-13+145C>A (NGF)	ENSP00000505558.1:n.-13+145C>A
ENST00000681124.1:c.-421+145C>A (NGF)	ENSP00000506364.1:n.-421+145C>A
ENST00000369512.2:c.-13+145C>A (NGF)	ENSP00000358525.2:n.-13+145C>A
NM_002506.2:c.-13+145C>A , LRG_260t1:c.-13+145C>A (NGF)	NP_002497.2:n.-13+145C>A
XM_006710663.2:c.-12-6675C>A (NGF)	XP_006710726.1:n.-12-6675C>A
XM_006710665.2:c.-13+145C>A (NGF)	XP_006710728.1:n.-13+145C>A
XM_011541518.1:c.153+145C>A (NGF)	XP_011539820.1:n.153+145C>A
NR_157569.1:n.207+10242G>T (NGF-AS1)
XM_006710663.3:c.-12-6675C>A (NGF)	XP_006710726.1:n.-12-6675C>A
XM_011541518.2:c.153+145C>A (NGF)	XP_011539820.1:n.153+145C>A
NM_002506.3:c.-13+145C>A (NGF) MANE Select	NP_002497.2:n.-13+145C>A