Canonical Allele Identifier: CA2059243040

Gene: IGF1 LINC02456

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102419619G= , CM000674.2:g.102419619G=	GRCh38
NC_000012.11:g.102813397G= , CM000674.1:g.102813397G=	GRCh37
NC_000012.10:g.101337527G=	NCBI36
NG_011713.1:g.65982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337514.11:c.292C= (IGF1) MANE Select	ENSP00000337612.7:p.Arg98=
ENST00000392905.7:c.292C= (IGF1)	ENSP00000376638.3:p.Arg98=
ENST00000644491.1:c.292C= (IGF1)	ENSP00000494228.1:p.Arg98=
ENST00000307046.8:c.292C= (IGF1)	ENSP00000302665.8:p.Arg98=
ENST00000337514.10:c.292C= (IGF1)	ENSP00000337612.6:p.Arg98=
ENST00000392904.5:c.292C= (IGF1)	ENSP00000376637.1:p.Arg98=
ENST00000392905.6:c.235C= (IGF1)	ENSP00000376638.2:p.Arg79=
ENST00000424202.6:c.244C= (IGF1)	ENSP00000416811.2:p.Arg82=
ENST00000456098.5:c.292C= (IGF1)	ENSP00000394999.1:p.Arg98=
NM_000618.3:c.292C= (IGF1)	NP_000609.1:p.Arg98=
NM_000618.4:c.292C= (IGF1)	NP_000609.1:p.Arg98=
NM_001111283.1:c.292C= (IGF1)	NP_001104753.1:p.Arg98=
NM_001111283.2:c.292C= (IGF1)	NP_001104753.1:p.Arg98=
NM_001111284.1:c.244C= (IGF1)	NP_001104754.1:p.Arg82=
NM_001111285.1:c.292C= (IGF1)	NP_001104755.1:p.Arg98=
XR_944534.1:n.551C= (IGF1)
XR_944535.1:n.328C= (IGF1)
XR_944536.1:n.313C= (IGF1)
XR_945270.1:n.6576-3452G= (LINC02456)
XR_945271.1:n.5629-3452G= (LINC02456)
XR_945272.1:n.6576-3452G= (LINC02456)
XR_945273.1:n.6526-3452G= (LINC02456)
XR_945274.1:n.6252-3452G= (LINC02456)
XR_945275.1:n.6132-3452G= (LINC02456)
XR_945276.1:n.6104-3452G= (LINC02456)
XR_945277.1:n.2200-3452G= (LINC02456)
NM_001111285.2:c.292C= (IGF1)	NP_001104755.1:p.Arg98=
XM_017019259.1:c.343C= (IGF1)	XP_016874748.1:p.Arg115=
XM_017019261.1:c.244C= (IGF1)	XP_016874750.1:p.Arg82=
XM_017019262.2:c.343C= (IGF1)	XP_016874751.1:p.Arg115=
XM_017019263.2:c.343C= (IGF1)	XP_016874752.1:p.Arg115=
XR_001749285.1:n.3025-3452G= (LINC02456)
NM_000618.5:c.292C= (IGF1) MANE Select	NP_000609.1:p.Arg98=
NM_001111283.3:c.292C= (IGF1)	NP_001104753.1:p.Arg98=
NM_001111284.2:c.244C= (IGF1)	NP_001104754.1:p.Arg82=
NM_001111285.3:c.292C= (IGF1)	NP_001104755.1:p.Arg98=