Canonical Allele Identifier: CA2513612349

Gene: NGF NGF-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286613_115286616del , CM000663.2:g.115286613_115286616del	GRCh38
NC_000001.10:g.115829234_115829237del , CM000663.1:g.115829234_115829237del	GRCh37
NC_000001.9:g.115630757_115630760del	NCBI36
NG_007944.1:g.56621_56624del , LRG_260:g.56621_56624del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.180_183del (NGF) MANE Select	ENSP00000358525.2:p.Arg62TrpfsTer?
ENST00000675637.2:c.180_183del (NGF)	ENSP00000502831.1:p.Arg62TrpfsTer?
ENST00000676038.2:c.180_183del (NGF)	ENSP00000502380.1:p.Arg62TrpfsTer?
ENST00000679806.1:c.180_183del (NGF)	ENSP00000506492.1:p.Arg62TrpfsTer?
ENST00000680116.1:c.180_183del (NGF)	ENSP00000505694.1:p.Arg62TrpfsTer?
ENST00000680540.1:c.180_183del (NGF)	ENSP00000506569.1:p.Arg62TrpfsTer?
ENST00000680752.1:c.180_183del (NGF)	ENSP00000505558.1:p.Arg62TrpfsTer?
ENST00000681124.1:c.-292_-289del (NGF)	ENSP00000506364.1:n.-292_-289del
ENST00000369512.2:c.180_183del (NGF)	ENSP00000358525.2:p.Arg62TrpfsTer?
NM_002506.2:c.180_183del , LRG_260t1:c.180_183del (NGF)	NP_002497.2:p.Arg62TrpfsTer?
XM_006710663.2:c.180_183del (NGF)	XP_006710726.1:p.Arg62TrpfsTer?
XM_006710665.2:c.180_183del (NGF)	XP_006710728.1:p.Arg62TrpfsTer?
XM_011541518.1:c.345_348del (NGF)	XP_011539820.1:p.Arg117TrpfsTer?
NR_157569.1:n.207+3373_207+3376del (NGF-AS1)
XM_006710663.3:c.180_183del (NGF)	XP_006710726.1:p.Arg62TrpfsTer?
XM_011541518.2:c.345_348del (NGF)	XP_011539820.1:p.Arg117TrpfsTer?
NM_002506.3:c.180_183del (NGF) MANE Select	NP_002497.2:p.Arg62TrpfsTer?