Canonical Allele Identifier: CA1704468935

Gene: IGFBP3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45920318G= , CM000669.2:g.45920318G=	GRCh38
NC_000007.13:g.45959917G= , CM000669.1:g.45959917G=	GRCh37
NC_000007.12:g.45926442G=	NCBI36
NG_011508.1:g.5955C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000598.5:c.403+420C= MANE Select	NP_000589.2:n.403+420C=
ENST00000613132.5:c.403+420C= MANE Select	ENSP00000477772.2:n.403+420C=
NM_000598.4:c.403+420C=	NP_000589.2:n.403+420C=
NM_001013398.1:c.421+402C=	NP_001013416.1:n.421+402C=
NM_001013398.2:c.421+402C=	NP_001013416.1:n.421+402C=
ENST00000275521.10:c.403+420C=	ENSP00000275521.5:n.403+420C=
ENST00000381083.8:c.421+402C=	ENSP00000370473.4:n.421+402C=
ENST00000381083.9:c.421+402C=	ENSP00000370473.4:n.421+402C=
ENST00000381086.9:c.112+420C=	ENSP00000370476.4:n.112+420C=
ENST00000448817.1:c.73+1309C=	ENSP00000389668.1:n.73+1309C=
ENST00000460477.1:n.130+420C=
ENST00000465642.1:n.98C=
ENST00000613132.4:c.340+420C=	ENSP00000477772.1:n.340+420C=
ENST00000615754.4:c.319+420C=	ENSP00000480717.1:n.319+420C=