Canonical Allele Identifier: CA1141873807

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115286497G= , CM000663.2:g.115286497G= GRCh38
NC_000001.10:g.115829118G= , CM000663.1:g.115829118G= GRCh37
NC_000001.9:g.115630641G= NCBI36
NG_007944.1:g.56740C= , LRG_260:g.56740C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369512.3:c.299C= (NGF) MANE Select ENSP00000358525.2:p.Thr100=
ENST00000675637.2:c.299C= (NGF) ENSP00000502831.1:p.Thr100=
ENST00000676038.2:c.299C= (NGF) ENSP00000502380.1:p.Thr100=
ENST00000679806.1:c.299C= (NGF) ENSP00000506492.1:p.Thr100=
ENST00000680116.1:c.299C= (NGF) ENSP00000505694.1:p.Thr100=
ENST00000680540.1:c.299C= (NGF) ENSP00000506569.1:p.Thr100=
ENST00000680752.1:c.299C= (NGF) ENSP00000505558.1:p.Thr100=
ENST00000681124.1:c.-173C= (NGF) ENSP00000506364.1:n.-173C=
ENST00000369512.2:c.299C= (NGF) ENSP00000358525.2:p.Thr100=
NM_002506.2:c.299C= , LRG_260t1:c.299C= (NGF) NP_002497.2:p.Thr100=
XM_006710663.2:c.299C= (NGF) XP_006710726.1:p.Thr100=
XM_006710665.2:c.299C= (NGF) XP_006710728.1:p.Thr100=
XM_011541518.1:c.464C= (NGF) XP_011539820.1:p.Thr155=
NR_157569.1:n.207+3257G= (NGF-AS1)
XM_006710663.3:c.299C= (NGF) XP_006710726.1:p.Thr100=
XM_011541518.2:c.464C= (NGF) XP_011539820.1:p.Thr155=
NM_002506.3:c.299C= (NGF) MANE Select NP_002497.2:p.Thr100=