Canonical Allele Identifier: CA1190533524

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115286612G= , CM000663.2:g.115286612G= GRCh38
NC_000001.10:g.115829233G= , CM000663.1:g.115829233G= GRCh37
NC_000001.9:g.115630756G= NCBI36
NG_007944.1:g.56625C= , LRG_260:g.56625C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369512.3:c.184C= (NGF) MANE Select ENSP00000358525.2:p.Arg62=
ENST00000675637.2:c.184C= (NGF) ENSP00000502831.1:p.Arg62=
ENST00000676038.2:c.184C= (NGF) ENSP00000502380.1:p.Arg62=
ENST00000679806.1:c.184C= (NGF) ENSP00000506492.1:p.Arg62=
ENST00000680116.1:c.184C= (NGF) ENSP00000505694.1:p.Arg62=
ENST00000680540.1:c.184C= (NGF) ENSP00000506569.1:p.Arg62=
ENST00000680752.1:c.184C= (NGF) ENSP00000505558.1:p.Arg62=
ENST00000681124.1:c.-288C= (NGF) ENSP00000506364.1:n.-288C=
ENST00000369512.2:c.184C= (NGF) ENSP00000358525.2:p.Arg62=
NM_002506.2:c.184C= , LRG_260t1:c.184C= (NGF) NP_002497.2:p.Arg62=
XM_006710663.2:c.184C= (NGF) XP_006710726.1:p.Arg62=
XM_006710665.2:c.184C= (NGF) XP_006710728.1:p.Arg62=
XM_011541518.1:c.349C= (NGF) XP_011539820.1:p.Arg117=
NR_157569.1:n.207+3372G= (NGF-AS1)
XM_006710663.3:c.184C= (NGF) XP_006710726.1:p.Arg62=
XM_011541518.2:c.349C= (NGF) XP_011539820.1:p.Arg117=
NM_002506.3:c.184C= (NGF) MANE Select NP_002497.2:p.Arg62=