Canonical Allele Identifier: CA1139773132

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115286692G= , CM000663.2:g.115286692G= GRCh38
NC_000001.10:g.115829313G= , CM000663.1:g.115829313G= GRCh37
NC_000001.9:g.115630836G= NCBI36
NG_007944.1:g.56545C= , LRG_260:g.56545C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369512.3:c.104C= (NGF) MANE Select ENSP00000358525.2:p.Ala35=
ENST00000675637.2:c.104C= (NGF) ENSP00000502831.1:p.Ala35=
ENST00000676038.2:c.104C= (NGF) ENSP00000502380.1:p.Ala35=
ENST00000679806.1:c.104C= (NGF) ENSP00000506492.1:p.Ala35=
ENST00000680116.1:c.104C= (NGF) ENSP00000505694.1:p.Ala35=
ENST00000680540.1:c.104C= (NGF) ENSP00000506569.1:p.Ala35=
ENST00000680752.1:c.104C= (NGF) ENSP00000505558.1:p.Ala35=
ENST00000681124.1:c.-368C= (NGF) ENSP00000506364.1:n.-368C=
ENST00000369512.2:c.104C= (NGF) ENSP00000358525.2:p.Ala35=
NM_002506.2:c.104C= , LRG_260t1:c.104C= (NGF) NP_002497.2:p.Ala35=
XM_006710663.2:c.104C= (NGF) XP_006710726.1:p.Ala35=
XM_006710665.2:c.104C= (NGF) XP_006710728.1:p.Ala35=
XM_011541518.1:c.269C= (NGF) XP_011539820.1:p.Ala90=
NR_157569.1:n.207+3452G= (NGF-AS1)
XM_006710663.3:c.104C= (NGF) XP_006710726.1:p.Ala35=
XM_011541518.2:c.269C= (NGF) XP_011539820.1:p.Ala90=
NM_002506.3:c.104C= (NGF) MANE Select NP_002497.2:p.Ala35=