Canonical Allele Identifier: CA2059268649

Gene: IGF1 LINC02456

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102462924C>T , CM000674.2:g.102462924C>T	GRCh38
NC_000012.11:g.102856702C>T , CM000674.1:g.102856702C>T	GRCh37
NC_000012.10:g.101380832C>T	NCBI36
NG_011713.1:g.22677G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337514.11:c.220+12719G>A (IGF1) MANE Select	ENSP00000337612.7:n.220+12719G>A
ENST00000392905.7:c.220+12719G>A (IGF1)	ENSP00000376638.3:n.220+12719G>A
ENST00000644491.1:c.220+12719G>A (IGF1)	ENSP00000494228.1:n.220+12719G>A
ENST00000307046.8:c.220+12719G>A (IGF1)	ENSP00000302665.8:n.220+12719G>A
ENST00000337514.10:c.220+12719G>A (IGF1)	ENSP00000337612.6:n.220+12719G>A
ENST00000392904.5:c.220+12719G>A (IGF1)	ENSP00000376637.1:n.220+12719G>A
ENST00000392905.6:c.163+12719G>A (IGF1)	ENSP00000376638.2:n.163+12719G>A
ENST00000424202.6:c.172+12719G>A (IGF1)	ENSP00000416811.2:n.172+12719G>A
ENST00000456098.5:c.220+12719G>A (IGF1)	ENSP00000394999.1:n.220+12719G>A
NM_000618.3:c.220+12719G>A (IGF1)	NP_000609.1:n.220+12719G>A
NM_000618.4:c.220+12719G>A (IGF1)	NP_000609.1:n.220+12719G>A
NM_001111283.1:c.220+12719G>A (IGF1)	NP_001104753.1:n.220+12719G>A
NM_001111283.2:c.220+12719G>A (IGF1)	NP_001104753.1:n.220+12719G>A
NM_001111284.1:c.172+12719G>A (IGF1)	NP_001104754.1:n.172+12719G>A
NM_001111285.1:c.220+12719G>A (IGF1)	NP_001104755.1:n.220+12719G>A
XR_944534.1:n.479+12719G>A (IGF1)
XR_944535.1:n.256+12719G>A (IGF1)
XR_944536.1:n.241+12719G>A (IGF1)
XR_945270.1:n.6882C>T (LINC02456)
XR_945271.1:n.5935C>T (LINC02456)
XR_945273.1:n.6832C>T (LINC02456)
XR_945274.1:n.6558C>T (LINC02456)
XR_945275.1:n.6438C>T (LINC02456)
XR_945276.1:n.6410C>T (LINC02456)
XR_945277.1:n.2506C>T (LINC02456)
NM_001111285.2:c.220+12719G>A (IGF1)	NP_001104755.1:n.220+12719G>A
XM_017019259.1:c.271+12719G>A (IGF1)	XP_016874748.1:n.271+12719G>A
XM_017019261.1:c.172+12719G>A (IGF1)	XP_016874750.1:n.172+12719G>A
XM_017019262.2:c.271+12719G>A (IGF1)	XP_016874751.1:n.271+12719G>A
XM_017019263.2:c.271+12719G>A (IGF1)	XP_016874752.1:n.271+12719G>A
XR_001749285.1:n.3331C>T (LINC02456)
NM_000618.5:c.220+12719G>A (IGF1) MANE Select	NP_000609.1:n.220+12719G>A
NM_001111283.3:c.220+12719G>A (IGF1)	NP_001104753.1:n.220+12719G>A
NM_001111284.2:c.172+12719G>A (IGF1)	NP_001104754.1:n.172+12719G>A
NM_001111285.3:c.220+12719G>A (IGF1)	NP_001104755.1:n.220+12719G>A