Canonical Allele Identifier: CA1143651790

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115286611C= , CM000663.2:g.115286611C= GRCh38
NC_000001.10:g.115829232C= , CM000663.1:g.115829232C= GRCh37
NC_000001.9:g.115630755C= NCBI36
NG_007944.1:g.56626G= , LRG_260:g.56626G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369512.3:c.185G= (NGF) MANE Select ENSP00000358525.2:p.Arg62=
ENST00000675637.2:c.185G= (NGF) ENSP00000502831.1:p.Arg62=
ENST00000676038.2:c.185G= (NGF) ENSP00000502380.1:p.Arg62=
ENST00000679806.1:c.185G= (NGF) ENSP00000506492.1:p.Arg62=
ENST00000680116.1:c.185G= (NGF) ENSP00000505694.1:p.Arg62=
ENST00000680540.1:c.185G= (NGF) ENSP00000506569.1:p.Arg62=
ENST00000680752.1:c.185G= (NGF) ENSP00000505558.1:p.Arg62=
ENST00000681124.1:c.-287G= (NGF) ENSP00000506364.1:n.-287G=
ENST00000369512.2:c.185G= (NGF) ENSP00000358525.2:p.Arg62=
NM_002506.2:c.185G= , LRG_260t1:c.185G= (NGF) NP_002497.2:p.Arg62=
XM_006710663.2:c.185G= (NGF) XP_006710726.1:p.Arg62=
XM_006710665.2:c.185G= (NGF) XP_006710728.1:p.Arg62=
XM_011541518.1:c.350G= (NGF) XP_011539820.1:p.Arg117=
NR_157569.1:n.207+3371C= (NGF-AS1)
XM_006710663.3:c.185G= (NGF) XP_006710726.1:p.Arg62=
XM_011541518.2:c.350G= (NGF) XP_011539820.1:p.Arg117=
NM_002506.3:c.185G= (NGF) MANE Select NP_002497.2:p.Arg62=