Canonical Allele Identifier: CA1676853857
Gene: IGF2R HGNC NCBI

Linked Data

dbSNP Id: rs1784304019

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160009721_160009723del , CM000668.2:g.160009721_160009723del GRCh38
NC_000006.11:g.160430753_160430755del , CM000668.1:g.160430753_160430755del GRCh37
NC_000006.10:g.160350743_160350745del NCBI36
NG_011785.3:g.45623_45625del
NG_011785.4:g.45623_45625del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356956.6:c.414+587_414+589del MANE Select ENSP00000349437.1:n.414+587_414+589del
ENST00000676781.1:c.414+587_414+589del ENSP00000504419.1:n.414+587_414+589del
ENST00000677704.1:c.414+587_414+589del ENSP00000503314.1:n.414+587_414+589del
ENST00000356956.5:c.414+587_414+589del ENSP00000349437.1:n.414+587_414+589del
NM_000876.2:c.414+587_414+589del NP_000867.2:n.414+587_414+589del
XR_942419.1:n.429+587_429+589del
NM_000876.3:c.414+587_414+589del NP_000867.2:n.414+587_414+589del
NM_000876.4:c.414+587_414+589del MANE Select NP_000867.3:n.414+587_414+589del