Canonical Allele Identifier: CA7751694
Community Standard Title: NM_000875.5(IGF1R):c.15C>T (p.Ser5=)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98649596C>T , CM000677.2:g.98649596C>T GRCh38
NC_000015.9:g.99192825C>T , CM000677.1:g.99192825C>T GRCh37
NC_000015.8:g.97010348C>T NCBI36
NG_009492.1:g.5065C>T
NG_045221.1:g.6626G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000875.5:c.15C>T (IGF1R) MANE Select NP_000866.1:p.Ser5=
ENST00000650285.1:c.15C>T (IGF1R) MANE Select ENSP00000497069.1:p.Ser5=
NM_000875.4:c.15C>T (IGF1R) NP_000866.1:p.Ser5=
NM_001291858.1:c.15C>T (IGF1R) NP_001278787.1:p.Ser5=
NM_001291858.2:c.15C>T (IGF1R) NP_001278787.1:p.Ser5=
NR_126453.1:n.1626G>A (IRAIN)
NR_126453.2:n.1192G>A (IRAIN)
ENST00000268035.10:c.15C>T (IGF1R) ENSP00000268035.6:p.Ser5=
ENST00000558762.5:c.15C>T (IGF1R) ENSP00000453007.1:p.Ser5=
ENST00000559925.5:n.15C>T (IGF1R)
ENST00000649865.1:c.15C>T (IGF1R) ENSP00000496919.1:p.Ser5=
XM_011521513.1:c.15C>T (IGF1R) XP_011519815.1:p.Ser5=
XM_011521514.1:c.15C>T (IGF1R) XP_011519816.1:p.Ser5=
XM_011521515.1:c.15C>T (IGF1R) XP_011519817.1:p.Ser5=