Canonical Allele Identifier: CA2551056711

Gene: NGF NGF-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286609_115286610insCCTG , CM000663.2:g.115286609_115286610insCCTG	GRCh38
NC_000001.10:g.115829230_115829231insCCTG , CM000663.1:g.115829230_115829231insCCTG	GRCh37
NC_000001.9:g.115630753_115630754insCCTG	NCBI36
NG_007944.1:g.56627_56628insCAGG , LRG_260:g.56627_56628insCAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000369512.3:c.186_187insCAGG (NGF) MANE Select	ENSP00000358525.2:p.Val63GlnfsTer17
ENST00000675637.2:c.186_187insCAGG (NGF)	ENSP00000502831.1:p.Val63GlnfsTer17
ENST00000676038.2:c.186_187insCAGG (NGF)	ENSP00000502380.1:p.Val63GlnfsTer17
ENST00000679806.1:c.186_187insCAGG (NGF)	ENSP00000506492.1:p.Val63GlnfsTer17
ENST00000680116.1:c.186_187insCAGG (NGF)	ENSP00000505694.1:p.Val63GlnfsTer17
ENST00000680540.1:c.186_187insCAGG (NGF)	ENSP00000506569.1:p.Val63GlnfsTer17
ENST00000680752.1:c.186_187insCAGG (NGF)	ENSP00000505558.1:p.Val63GlnfsTer17
ENST00000681124.1:c.-286_-285insCAGG (NGF)	ENSP00000506364.1:n.-286_-285insCAGG
ENST00000369512.2:c.186_187insCAGG (NGF)	ENSP00000358525.2:p.Val63GlnfsTer17
NM_002506.2:c.186_187insCAGG , LRG_260t1:c.186_187insCAGG (NGF)	NP_002497.2:p.Val63GlnfsTer17
XM_006710663.2:c.186_187insCAGG (NGF)	XP_006710726.1:p.Val63GlnfsTer17
XM_006710665.2:c.186_187insCAGG (NGF)	XP_006710728.1:p.Val63GlnfsTer17
XM_011541518.1:c.351_352insCAGG (NGF)	XP_011539820.1:p.Val118GlnfsTer17
NR_157569.1:n.207+3369_207+3370insCCTG (NGF-AS1)
XM_006710663.3:c.186_187insCAGG (NGF)	XP_006710726.1:p.Val63GlnfsTer17
XM_011541518.2:c.351_352insCAGG (NGF)	XP_011539820.1:p.Val118GlnfsTer17
NM_002506.3:c.186_187insCAGG (NGF) MANE Select	NP_002497.2:p.Val63GlnfsTer17