Canonical Allele Identifier: CA2059252822

Gene: IGF1 LINC02456

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102405458C>G , CM000674.2:g.102405458C>G	GRCh38
NC_000012.11:g.102799236C>G , CM000674.1:g.102799236C>G	GRCh37
NC_000012.10:g.101323366C>G	NCBI36
NG_011713.1:g.80143G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000618.5:c.403-2892G>C (IGF1) MANE Select	NP_000609.1:n.403-2892G>C
ENST00000337514.11:c.403-2892G>C (IGF1) MANE Select	ENSP00000337612.7:n.403-2892G>C
NM_000618.3:c.403-2892G>C (IGF1)	NP_000609.1:n.403-2892G>C
NM_000618.4:c.403-2892G>C (IGF1)	NP_000609.1:n.403-2892G>C
NM_001111283.1:c.452-2892G>C (IGF1)	NP_001104753.1:n.452-2892G>C
NM_001111283.2:c.452-2892G>C (IGF1)	NP_001104753.1:n.452-2892G>C
NM_001111283.3:c.452-2892G>C (IGF1)	NP_001104753.1:n.452-2892G>C
NM_001111284.1:c.355-2892G>C (IGF1)	NP_001104754.1:n.355-2892G>C
NM_001111284.2:c.355-2892G>C (IGF1)	NP_001104754.1:n.355-2892G>C
ENST00000337514.10:c.403-2892G>C (IGF1)	ENSP00000337612.6:n.403-2892G>C
ENST00000392904.5:c.452-2892G>C (IGF1)	ENSP00000376637.1:n.452-2892G>C
ENST00000392905.6:c.395-2892G>C (IGF1)	ENSP00000376638.2:n.395-2892G>C
ENST00000392905.7:c.452-2892G>C (IGF1)	ENSP00000376638.3:n.452-2892G>C
ENST00000424202.6:c.355-2892G>C (IGF1)	ENSP00000416811.2:n.355-2892G>C
ENST00000456098.5:c.452-2892G>C (IGF1)	ENSP00000394999.1:n.452-2892G>C
ENST00000481539.1:n.44-2892G>C (IGF1)
ENST00000644491.1:c.403-2892G>C (IGF1)	ENSP00000494228.1:n.403-2892G>C
XM_017019262.2:c.503-2892G>C (IGF1)	XP_016874751.1:n.503-2892G>C
XM_017019263.2:c.454-2892G>C (IGF1)	XP_016874752.1:n.454-2892G>C
XR_001749285.1:n.815+1227C>G (LINC02456)
XR_001749286.1:n.376+1227C>G (LINC02456)
XR_001749287.1:n.694+1227C>G (LINC02456)
XR_001749288.1:n.1703+1227C>G (LINC02456)
XR_944534.1:n.2962-2892G>C (IGF1)
XR_944535.1:n.2739-2892G>C (IGF1)
XR_944536.1:n.2724-2892G>C (IGF1)
XR_945270.1:n.700+1227C>G (LINC02456)
XR_945271.1:n.700+1227C>G (LINC02456)
XR_945272.1:n.700+1227C>G (LINC02456)
XR_945273.1:n.650+1227C>G (LINC02456)
XR_945274.1:n.376+1227C>G (LINC02456)
XR_945275.1:n.256+1227C>G (LINC02456)
XR_945276.1:n.228+1227C>G (LINC02456)
XR_945277.1:n.700+1227C>G (LINC02456)