Canonical Allele Identifier: CA1023050

Gene: NGF NGF-AS1

Linked Data

• dbSNP Id: rs768548505
• ExAC: 1:115829250 GCCGGGGC / G
• gnomAD v2: 1-115829250-GCCGGGGC-G
• gnomAD v4: 1-115286629-GCCGGGGC-G
• MyVariant Identifiers: chr1:g.115829251_115829257del (hg19) ; chr1:g.115286630_115286636del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286630_115286636del , CM000663.2:g.115286630_115286636del	GRCh38
NC_000001.10:g.115829251_115829257del , CM000663.1:g.115829251_115829257del	GRCh37
NC_000001.9:g.115630774_115630780del	NCBI36
NG_007944.1:g.56601_56607del , LRG_260:g.56601_56607del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.160_166del (NGF) MANE Select	ENSP00000358525.2:p.Ala54GlnfsTer4
ENST00000675637.2:c.160_166del (NGF)	ENSP00000502831.1:p.Ala54GlnfsTer4
ENST00000676038.2:c.160_166del (NGF)	ENSP00000502380.1:p.Ala54GlnfsTer4
ENST00000679806.1:c.160_166del (NGF)	ENSP00000506492.1:p.Ala54GlnfsTer4
ENST00000680116.1:c.160_166del (NGF)	ENSP00000505694.1:p.Ala54GlnfsTer4
ENST00000680540.1:c.160_166del (NGF)	ENSP00000506569.1:p.Ala54GlnfsTer4
ENST00000680752.1:c.160_166del (NGF)	ENSP00000505558.1:p.Ala54GlnfsTer4
ENST00000681124.1:c.-312_-306del (NGF)	ENSP00000506364.1:n.-312_-306del
ENST00000369512.2:c.160_166del (NGF)	ENSP00000358525.2:p.Ala54GlnfsTer4
NM_002506.2:c.160_166del , LRG_260t1:c.160_166del (NGF)	NP_002497.2:p.Ala54GlnfsTer4
XM_006710663.2:c.160_166del (NGF)	XP_006710726.1:p.Ala54GlnfsTer4
XM_006710665.2:c.160_166del (NGF)	XP_006710728.1:p.Ala54GlnfsTer4
XM_011541518.1:c.325_331del (NGF)	XP_011539820.1:p.Ala109GlnfsTer4
NR_157569.1:n.207+3390_207+3396del (NGF-AS1)
XM_006710663.3:c.160_166del (NGF)	XP_006710726.1:p.Ala54GlnfsTer4
XM_011541518.2:c.325_331del (NGF)	XP_011539820.1:p.Ala109GlnfsTer4
NM_002506.3:c.160_166del (NGF) MANE Select	NP_002497.2:p.Ala54GlnfsTer4