Canonical Allele Identifier: CA1676853856
Gene: IGF2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160009717_160009720delinsAAAT , CM000668.2:g.160009717_160009720delinsAAAT GRCh38
NC_000006.11:g.160430749_160430752delinsAAAT , CM000668.1:g.160430749_160430752delinsAAAT GRCh37
NC_000006.10:g.160350739_160350742delinsAAAT NCBI36
NG_011785.3:g.45619_45622delinsAAAT
NG_011785.4:g.45619_45622delinsAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000356956.6:c.414+583_414+586delinsAAAT MANE Select ENSP00000349437.1:n.414+583_414+586delinsAAAT
ENST00000676781.1:c.414+583_414+586delinsAAAT ENSP00000504419.1:n.414+583_414+586delinsAAAT
ENST00000677704.1:c.414+583_414+586delinsAAAT ENSP00000503314.1:n.414+583_414+586delinsAAAT
ENST00000356956.5:c.414+583_414+586delinsAAAT ENSP00000349437.1:n.414+583_414+586delinsAAAT
NM_000876.2:c.414+583_414+586delinsAAAT NP_000867.2:n.414+583_414+586delinsAAAT
XR_942419.1:n.429+583_429+586delinsAAAT
NM_000876.3:c.414+583_414+586delinsAAAT NP_000867.2:n.414+583_414+586delinsAAAT
NM_000876.4:c.414+583_414+586delinsAAAT MANE Select NP_000867.3:n.414+583_414+586delinsAAAT