Canonical Allele Identifier: CA1704466169

Gene: IGFBP3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45913882_45913883delinsCA , CM000669.2:g.45913882_45913883delinsCA	GRCh38
NC_000007.13:g.45953481_45953482delinsCA , CM000669.1:g.45953481_45953482delinsCA	GRCh37
NC_000007.12:g.45920006_45920007delinsCA	NCBI36
NG_011508.1:g.12390_12391delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613132.5:c.*16-49_*16-48delinsTG MANE Select	ENSP00000477772.2:n.*16-49_*16-48delinsTG
ENST00000381083.9:c.*16-49_*16-48delinsTG	ENSP00000370473.4:n.*16-49_*16-48delinsTG
ENST00000275521.10:c.*16-49_*16-48delinsTG	ENSP00000275521.5:n.*16-49_*16-48delinsTG
ENST00000381083.8:c.*16-49_*16-48delinsTG	ENSP00000370473.4:n.*16-49_*16-48delinsTG
ENST00000381086.9:c.*16-49_*16-48delinsTG	ENSP00000370476.4:n.*16-49_*16-48delinsTG
ENST00000460209.1:n.522-49_522-48delinsTG
ENST00000613132.4:c.829-49_829-48delinsTG	ENSP00000477772.1:n.829-49_829-48delinsTG
NM_000598.4:c.*16-49_*16-48delinsTG	NP_000589.2:n.*16-49_*16-48delinsTG
NM_001013398.1:c.*16-49_*16-48delinsTG	NP_001013416.1:n.*16-49_*16-48delinsTG
NM_001013398.2:c.*16-49_*16-48delinsTG	NP_001013416.1:n.*16-49_*16-48delinsTG
NM_000598.5:c.*16-49_*16-48delinsTG MANE Select	NP_000589.2:n.*16-49_*16-48delinsTG