Canonical Allele Identifier: CA1704466151

Gene: IGFBP3

Linked Data

• dbSNP Id: rs1784574630

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45913853_45913856del , CM000669.2:g.45913853_45913856del	GRCh38
NC_000007.13:g.45953452_45953455del , CM000669.1:g.45953452_45953455del	GRCh37
NC_000007.12:g.45919977_45919980del	NCBI36
NG_011508.1:g.12420_12423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613132.5:c.*16-19_*16-16del MANE Select	ENSP00000477772.2:n.*16-19_*16-16del
ENST00000381083.9:c.*16-19_*16-16del	ENSP00000370473.4:n.*16-19_*16-16del
ENST00000275521.10:c.*16-19_*16-16del	ENSP00000275521.5:n.*16-19_*16-16del
ENST00000381083.8:c.*16-19_*16-16del	ENSP00000370473.4:n.*16-19_*16-16del
ENST00000381086.9:c.*16-19_*16-16del	ENSP00000370476.4:n.*16-19_*16-16del
ENST00000460209.1:n.522-19_522-16del
ENST00000613132.4:c.829-19_829-16del	ENSP00000477772.1:n.829-19_829-16del
NM_000598.4:c.*16-19_*16-16del	NP_000589.2:n.*16-19_*16-16del
NM_001013398.1:c.*16-19_*16-16del	NP_001013416.1:n.*16-19_*16-16del
NM_001013398.2:c.*16-19_*16-16del	NP_001013416.1:n.*16-19_*16-16del
NM_000598.5:c.*16-19_*16-16del MANE Select	NP_000589.2:n.*16-19_*16-16del