Canonical Allele Identifier: CA2059244239

Gene: IGF1 LINC02456

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102396074C= , CM000674.2:g.102396074C=	GRCh38
NC_000012.11:g.102789852C= , CM000674.1:g.102789852C=	GRCh37
NC_000012.10:g.101313982C=	NCBI36
NG_011713.1:g.89527G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000618.5:c.*6433G= (IGF1) MANE Select	NP_000609.1:n.*6433G=
ENST00000337514.11:c.*6433G= (IGF1) MANE Select	ENSP00000337612.7:n.*6433G=
NM_000618.3:c.*6433G= (IGF1)	NP_000609.1:n.*6433G=
NM_000618.4:c.*6433G= (IGF1)	NP_000609.1:n.*6433G=
NM_001111283.1:c.*6467G= (IGF1)	NP_001104753.1:n.*6467G=
NM_001111283.2:c.*6467G= (IGF1)	NP_001104753.1:n.*6467G=
NM_001111283.3:c.*6467G= (IGF1)	NP_001104753.1:n.*6467G=
NM_001111284.1:c.*6433G= (IGF1)	NP_001104754.1:n.*6433G=
NM_001111284.2:c.*6433G= (IGF1)	NP_001104754.1:n.*6433G=
ENST00000337514.10:c.*6433G= (IGF1)	ENSP00000337612.6:n.*6433G=
ENST00000456098.5:c.*6467G= (IGF1)	ENSP00000394999.1:n.*6467G=
XM_017019262.2:c.*6467G= (IGF1)	XP_016874751.1:n.*6467G=
XM_017019263.2:c.*6433G= (IGF1)	XP_016874752.1:n.*6433G=
XR_001749285.1:n.697-8039C= (LINC02456)
XR_001749286.1:n.258-8039C= (LINC02456)
XR_001749287.1:n.576-8039C= (LINC02456)
XR_001749288.1:n.1585-8039C= (LINC02456)
XR_945270.1:n.582-8039C= (LINC02456)
XR_945271.1:n.582-8039C= (LINC02456)
XR_945272.1:n.582-8039C= (LINC02456)
XR_945273.1:n.532-8039C= (LINC02456)
XR_945274.1:n.258-8039C= (LINC02456)
XR_945275.1:n.138-8039C= (LINC02456)
XR_945276.1:n.110-8039C= (LINC02456)
XR_945277.1:n.582-8039C= (LINC02456)