Canonical Allele Identifier: CA15763475

Gene: IGF1 LINC02456

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102462696A>G , CM000674.2:g.102462696A>G	GRCh38
NC_000012.11:g.102856474A>G , CM000674.1:g.102856474A>G	GRCh37
NC_000012.10:g.101380604A>G	NCBI36
NG_011713.1:g.22905T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337514.11:c.220+12947T>C (IGF1) MANE Select	ENSP00000337612.7:n.220+12947T>C
ENST00000392905.7:c.220+12947T>C (IGF1)	ENSP00000376638.3:n.220+12947T>C
ENST00000644491.1:c.220+12947T>C (IGF1)	ENSP00000494228.1:n.220+12947T>C
ENST00000307046.8:c.220+12947T>C (IGF1)	ENSP00000302665.8:n.220+12947T>C
ENST00000337514.10:c.220+12947T>C (IGF1)	ENSP00000337612.6:n.220+12947T>C
ENST00000392904.5:c.220+12947T>C (IGF1)	ENSP00000376637.1:n.220+12947T>C
ENST00000392905.6:c.163+12947T>C (IGF1)	ENSP00000376638.2:n.163+12947T>C
ENST00000424202.6:c.172+12947T>C (IGF1)	ENSP00000416811.2:n.172+12947T>C
ENST00000456098.5:c.220+12947T>C (IGF1)	ENSP00000394999.1:n.220+12947T>C
NM_000618.3:c.220+12947T>C (IGF1)	NP_000609.1:n.220+12947T>C
NM_000618.4:c.220+12947T>C (IGF1)	NP_000609.1:n.220+12947T>C
NM_001111283.1:c.220+12947T>C (IGF1)	NP_001104753.1:n.220+12947T>C
NM_001111283.2:c.220+12947T>C (IGF1)	NP_001104753.1:n.220+12947T>C
NM_001111284.1:c.172+12947T>C (IGF1)	NP_001104754.1:n.172+12947T>C
NM_001111285.1:c.220+12947T>C (IGF1)	NP_001104755.1:n.220+12947T>C
XR_944534.1:n.479+12947T>C (IGF1)
XR_944535.1:n.256+12947T>C (IGF1)
XR_944536.1:n.241+12947T>C (IGF1)
XR_945270.1:n.6686-32A>G (LINC02456)
XR_945271.1:n.5739-32A>G (LINC02456)
XR_945273.1:n.6636-32A>G (LINC02456)
XR_945274.1:n.6362-32A>G (LINC02456)
XR_945275.1:n.6242-32A>G (LINC02456)
XR_945276.1:n.6214-32A>G (LINC02456)
XR_945277.1:n.2310-32A>G (LINC02456)
NM_001111285.2:c.220+12947T>C (IGF1)	NP_001104755.1:n.220+12947T>C
XM_017019259.1:c.271+12947T>C (IGF1)	XP_016874748.1:n.271+12947T>C
XM_017019261.1:c.172+12947T>C (IGF1)	XP_016874750.1:n.172+12947T>C
XM_017019262.2:c.271+12947T>C (IGF1)	XP_016874751.1:n.271+12947T>C
XM_017019263.2:c.271+12947T>C (IGF1)	XP_016874752.1:n.271+12947T>C
XR_001749285.1:n.3135-32A>G (LINC02456)
NM_000618.5:c.220+12947T>C (IGF1) MANE Select	NP_000609.1:n.220+12947T>C
NM_001111283.3:c.220+12947T>C (IGF1)	NP_001104753.1:n.220+12947T>C
NM_001111284.2:c.172+12947T>C (IGF1)	NP_001104754.1:n.172+12947T>C
NM_001111285.3:c.220+12947T>C (IGF1)	NP_001104755.1:n.220+12947T>C