Canonical Allele Identifier: CA548608653

Gene: IGF2BP2

Linked Data

• gnomAD v2: 3-185512086-A-AG
• gnomAD v3: 3-185794298-A-AG
• gnomAD v4: 3-185794298-A-AG
• MyVariant Identifiers: chr3:g.185512086_185512087insG (hg19) ; chr3:g.185794298_185794299insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185794298_185794299insG , CM000665.2:g.185794298_185794299insG	GRCh38
NC_000003.11:g.185512086_185512087insG , CM000665.1:g.185512086_185512087insG	GRCh37
NC_000003.10:g.186994780_186994781insG	NCBI36
NG_011602.1:g.35741_35742insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382199.7:c.239+28854_239+28855insC MANE Select	ENSP00000371634.3:n.239+28854_239+28855insC
ENST00000346192.7:c.239+28854_239+28855insC	ENSP00000320204.5:n.239+28854_239+28855insC
ENST00000382199.6:c.239+28854_239+28855insC	ENSP00000371634.2:n.239+28854_239+28855insC
ENST00000421047.3:c.50+26713_50+26714insC	ENSP00000413787.3:n.50+26713_50+26714insC
ENST00000457616.6:c.239+28854_239+28855insC	ENSP00000410242.2:n.239+28854_239+28855insC
ENST00000461957.5:n.119+28854_119+28855insC
ENST00000466476.1:n.171+28854_171+28855insC
ENST00000493302.5:n.120+26713_120+26714insC
NM_001007225.1:c.239+28854_239+28855insC	NP_001007226.1:n.239+28854_239+28855insC
NM_001291869.1:c.239+28854_239+28855insC	NP_001278798.1:n.239+28854_239+28855insC
NM_001291872.1:c.50+26713_50+26714insC	NP_001278801.1:n.50+26713_50+26714insC
NM_001291873.1:c.50+26713_50+26714insC	NP_001278802.1:n.50+26713_50+26714insC
NM_001291874.1:c.50+26713_50+26714insC	NP_001278803.1:n.50+26713_50+26714insC
NM_001291875.1:c.-106+26713_-106+26714insC	NP_001278804.1:n.-106+26713_-106+26714insC
NM_006548.4:c.239+28854_239+28855insC	NP_006539.3:n.239+28854_239+28855insC
XM_011512338.1:c.239+28854_239+28855insC	XP_011510640.1:n.239+28854_239+28855insC
XM_011512339.1:c.239+28854_239+28855insC	XP_011510641.1:n.239+28854_239+28855insC
XM_011512341.1:c.239+28854_239+28855insC	XP_011510643.1:n.239+28854_239+28855insC
XR_427358.2:n.318+28854_318+28855insC
NM_001007225.2:c.239+28854_239+28855insC	NP_001007226.1:n.239+28854_239+28855insC
NM_001291869.2:c.239+28854_239+28855insC	NP_001278798.1:n.239+28854_239+28855insC
NM_001291872.2:c.50+26713_50+26714insC	NP_001278801.1:n.50+26713_50+26714insC
NM_001291873.2:c.50+26713_50+26714insC	NP_001278802.1:n.50+26713_50+26714insC
NM_001291874.2:c.50+26713_50+26714insC	NP_001278803.1:n.50+26713_50+26714insC
NM_001291875.2:c.-106+26713_-106+26714insC	NP_001278804.1:n.-106+26713_-106+26714insC
NM_006548.5:c.239+28854_239+28855insC	NP_006539.3:n.239+28854_239+28855insC
NR_138486.1:n.335+28854_335+28855insC
XM_017005557.2:c.178+30484_178+30485insC	XP_016861046.1:n.178+30484_178+30485insC
XM_017005558.2:c.239+28854_239+28855insC	XP_016861047.1:n.239+28854_239+28855insC
XM_017005559.2:c.239+28854_239+28855insC	XP_016861048.1:n.239+28854_239+28855insC
XM_017005560.2:c.35+28854_35+28855insC	XP_016861049.1:n.35+28854_35+28855insC
XM_017005561.1:c.239+28854_239+28855insC	XP_016861050.1:n.239+28854_239+28855insC
XM_017005562.1:c.239+28854_239+28855insC	XP_016861051.1:n.239+28854_239+28855insC
XM_017005563.1:c.239+28854_239+28855insC	XP_016861052.1:n.239+28854_239+28855insC
XM_017005564.1:c.239+28854_239+28855insC	XP_016861053.1:n.239+28854_239+28855insC
XM_024453316.1:c.-170+30484_-170+30485insC	XP_024309084.1:n.-170+30484_-170+30485insC
XR_001739984.2:n.324+28854_324+28855insC
NM_001007225.3:c.239+28854_239+28855insC	NP_001007226.1:n.239+28854_239+28855insC
NM_001291869.3:c.239+28854_239+28855insC	NP_001278798.1:n.239+28854_239+28855insC
NM_001291872.3:c.50+26713_50+26714insC	NP_001278801.1:n.50+26713_50+26714insC
NM_001291874.3:c.50+26713_50+26714insC	NP_001278803.1:n.50+26713_50+26714insC
NM_001291875.3:c.-106+26713_-106+26714insC	NP_001278804.1:n.-106+26713_-106+26714insC
NM_006548.6:c.239+28854_239+28855insC MANE Select	NP_006539.3:n.239+28854_239+28855insC
NR_138486.2:n.321+28854_321+28855insC
NM_001291873.3:c.50+26713_50+26714insC	NP_001278802.1:n.50+26713_50+26714insC