Canonical Allele Identifier: CA682842392

Gene: IGF1 LINC02456

Linked Data

• dbSNP Id: rs1220241170
• gnomAD v3: 12-102444819-CAT-C
• gnomAD v4: 12-102444819-CAT-C
• MyVariant Identifiers: chr12:g.102838598_102838599del (hg19) ; chr12:g.102444820_102444821del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102444821_102444822del , CM000674.2:g.102444821_102444822del	GRCh38
NC_000012.11:g.102838599_102838600del , CM000674.1:g.102838599_102838600del	GRCh37
NC_000012.10:g.101362729_101362730del	NCBI36
NG_011713.1:g.40780_40781del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337514.11:c.221-25131_221-25130del (IGF1) MANE Select	ENSP00000337612.7:n.221-25131_221-25130del
ENST00000392905.7:c.221-25131_221-25130del (IGF1)	ENSP00000376638.3:n.221-25131_221-25130del
ENST00000644491.1:c.221-25131_221-25130del (IGF1)	ENSP00000494228.1:n.221-25131_221-25130del
ENST00000307046.8:c.221-25131_221-25130del (IGF1)	ENSP00000302665.8:n.221-25131_221-25130del
ENST00000337514.10:c.221-25131_221-25130del (IGF1)	ENSP00000337612.6:n.221-25131_221-25130del
ENST00000392904.5:c.221-25131_221-25130del (IGF1)	ENSP00000376637.1:n.221-25131_221-25130del
ENST00000392905.6:c.164-25131_164-25130del (IGF1)	ENSP00000376638.2:n.164-25131_164-25130del
ENST00000424202.6:c.173-25131_173-25130del (IGF1)	ENSP00000416811.2:n.173-25131_173-25130del
ENST00000456098.5:c.221-25131_221-25130del (IGF1)	ENSP00000394999.1:n.221-25131_221-25130del
NM_000618.3:c.221-25131_221-25130del (IGF1)	NP_000609.1:n.221-25131_221-25130del
NM_000618.4:c.221-25131_221-25130del (IGF1)	NP_000609.1:n.221-25131_221-25130del
NM_001111283.1:c.221-25131_221-25130del (IGF1)	NP_001104753.1:n.221-25131_221-25130del
NM_001111283.2:c.221-25131_221-25130del (IGF1)	NP_001104753.1:n.221-25131_221-25130del
NM_001111284.1:c.173-25131_173-25130del (IGF1)	NP_001104754.1:n.173-25131_173-25130del
NM_001111285.1:c.221-25131_221-25130del (IGF1)	NP_001104755.1:n.221-25131_221-25130del
XR_944534.1:n.480-25131_480-25130del (IGF1)
XR_944535.1:n.257-25131_257-25130del (IGF1)
XR_944536.1:n.242-25131_242-25130del (IGF1)
XR_945270.1:n.6686-17907_6686-17906del (LINC02456)
XR_945271.1:n.5739-17907_5739-17906del (LINC02456)
XR_945272.1:n.6686-10966_6686-10965del (LINC02456)
XR_945273.1:n.6636-17907_6636-17906del (LINC02456)
XR_945274.1:n.6362-17907_6362-17906del (LINC02456)
XR_945275.1:n.6242-17907_6242-17906del (LINC02456)
XR_945276.1:n.6214-17907_6214-17906del (LINC02456)
XR_945277.1:n.2310-17907_2310-17906del (LINC02456)
NM_001111285.2:c.221-25131_221-25130del (IGF1)	NP_001104755.1:n.221-25131_221-25130del
XM_017019259.1:c.272-25131_272-25130del (IGF1)	XP_016874748.1:n.272-25131_272-25130del
XM_017019261.1:c.173-25131_173-25130del (IGF1)	XP_016874750.1:n.173-25131_173-25130del
XM_017019262.2:c.272-25131_272-25130del (IGF1)	XP_016874751.1:n.272-25131_272-25130del
XM_017019263.2:c.272-25131_272-25130del (IGF1)	XP_016874752.1:n.272-25131_272-25130del
XR_001749285.1:n.3135-17907_3135-17906del (LINC02456)
NM_000618.5:c.221-25131_221-25130del (IGF1) MANE Select	NP_000609.1:n.221-25131_221-25130del
NM_001111283.3:c.221-25131_221-25130del (IGF1)	NP_001104753.1:n.221-25131_221-25130del
NM_001111284.2:c.173-25131_173-25130del (IGF1)	NP_001104754.1:n.173-25131_173-25130del
NM_001111285.3:c.221-25131_221-25130del (IGF1)	NP_001104755.1:n.221-25131_221-25130del