Canonical Allele Identifier: CA7751724
Community Standard Title: NM_000875.5(IGF1R):c.94+15G>A

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98649690G>A , CM000677.2:g.98649690G>A GRCh38
NC_000015.9:g.99192919G>A , CM000677.1:g.99192919G>A GRCh37
NC_000015.8:g.97010442G>A NCBI36
NG_009492.1:g.5159G>A
NG_045221.1:g.6532C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000875.5:c.94+15G>A (IGF1R) MANE Select NP_000866.1:n.94+15G>A
ENST00000650285.1:c.94+15G>A (IGF1R) MANE Select ENSP00000497069.1:n.94+15G>A
NM_000875.4:c.94+15G>A (IGF1R) NP_000866.1:n.94+15G>A
NM_001291858.1:c.94+15G>A (IGF1R) NP_001278787.1:n.94+15G>A
NM_001291858.2:c.94+15G>A (IGF1R) NP_001278787.1:n.94+15G>A
NR_126453.1:n.1532C>T (IRAIN)
NR_126453.2:n.1098C>T (IRAIN)
ENST00000268035.10:c.94+15G>A (IGF1R) ENSP00000268035.6:n.94+15G>A
ENST00000558762.5:c.94+15G>A (IGF1R) ENSP00000453007.1:n.94+15G>A
ENST00000559925.5:n.94+15G>A (IGF1R)
ENST00000649865.1:c.94+15G>A (IGF1R) ENSP00000496919.1:n.94+15G>A
XM_011521513.1:c.94+15G>A (IGF1R) XP_011519815.1:n.94+15G>A
XM_011521514.1:c.94+15G>A (IGF1R) XP_011519816.1:n.94+15G>A
XM_011521515.1:c.94+15G>A (IGF1R) XP_011519817.1:n.94+15G>A