Canonical Allele Identifier: CA393696352
Community Standard Title: NM_000875.5(IGF1R):c.16G>C (p.Gly6Arg)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98649597G>C , CM000677.2:g.98649597G>C GRCh38
NC_000015.9:g.99192826G>C , CM000677.1:g.99192826G>C GRCh37
NC_000015.8:g.97010349G>C NCBI36
NG_009492.1:g.5066G>C
NG_045221.1:g.6625C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000875.5:c.16G>C (IGF1R) MANE Select NP_000866.1:p.Gly6Arg
ENST00000650285.1:c.16G>C (IGF1R) MANE Select ENSP00000497069.1:p.Gly6Arg
NM_000875.4:c.16G>C (IGF1R) NP_000866.1:p.Gly6Arg
NM_001291858.1:c.16G>C (IGF1R) NP_001278787.1:p.Gly6Arg
NM_001291858.2:c.16G>C (IGF1R) NP_001278787.1:p.Gly6Arg
NR_126453.1:n.1625C>G (IRAIN)
NR_126453.2:n.1191C>G (IRAIN)
ENST00000268035.10:c.16G>C (IGF1R) ENSP00000268035.6:p.Gly6Arg
ENST00000558762.5:c.16G>C (IGF1R) ENSP00000453007.1:p.Gly6Arg
ENST00000559925.5:n.16G>C (IGF1R)
ENST00000649865.1:c.16G>C (IGF1R) ENSP00000496919.1:p.Gly6Arg
XM_011521513.1:c.16G>C (IGF1R) XP_011519815.1:p.Gly6Arg
XM_011521514.1:c.16G>C (IGF1R) XP_011519816.1:p.Gly6Arg
XM_011521515.1:c.16G>C (IGF1R) XP_011519817.1:p.Gly6Arg