Canonical Allele Identifier: CA2199291020
Community Standard Title: NM_000875.5(IGF1R):c.*731C=
Gene: IGF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98958173C= , CM000677.2:g.98958173C= GRCh38
NC_000015.9:g.99501402C= , CM000677.1:g.99501402C= GRCh37
NC_000015.8:g.97318925C= NCBI36
NG_009492.1:g.313642C=

Transcript Alleles

HGVS Amino-acid Change
NM_000875.5:c.*731C= MANE Select NP_000866.1:n.*731C=
ENST00000650285.1:c.*731C= MANE Select ENSP00000497069.1:n.*731C=
NM_000875.4:c.*731C= NP_000866.1:n.*731C=
NM_001291858.1:c.*731C= NP_001278787.1:n.*731C=
NM_001291858.2:c.*731C= NP_001278787.1:n.*731C=
ENST00000268035.10:c.*731C= ENSP00000268035.6:n.*731C=
ENST00000558762.5:c.*731C= ENSP00000453007.1:n.*731C=
ENST00000649865.1:c.*731C= ENSP00000496919.1:n.*731C=
XM_011521513.1:c.*731C= XP_011519815.1:n.*731C=
XM_011521514.1:c.*245C= XP_011519816.1:n.*245C=
XM_011521515.1:c.*731C= XP_011519817.1:n.*731C=
XM_011521516.1:c.*731C= XP_011519818.1:n.*731C=
XM_011521516.2:c.*731C= XP_011519818.1:n.*731C=
XM_011521517.1:c.*731C= XP_011519819.1:n.*731C=
XM_011521517.2:c.*731C= XP_011519819.1:n.*731C=
XM_017022136.1:c.*731C= XP_016877625.1:n.*731C=
XM_017022137.1:c.*245C= XP_016877626.1:n.*245C=
XM_017022138.1:c.*731C= XP_016877627.1:n.*731C=
XM_017022139.1:c.*731C= XP_016877628.1:n.*731C=
XM_024449913.1:c.*731C= XP_024305681.1:n.*731C=