Canonical Allele Identifier: CA2059259493

Gene: IGF1 LINC02456

Linked Data

• dbSNP Id: rs7136446

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102444737C>A , CM000674.2:g.102444737C>A	GRCh38
NC_000012.11:g.102838515C>A , CM000674.1:g.102838515C>A	GRCh37
NC_000012.10:g.101362645C>A	NCBI36
NG_011713.1:g.40864G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000337514.11:c.221-25047G>T (IGF1) MANE Select	ENSP00000337612.7:n.221-25047G>T
ENST00000392905.7:c.221-25047G>T (IGF1)	ENSP00000376638.3:n.221-25047G>T
ENST00000644491.1:c.221-25047G>T (IGF1)	ENSP00000494228.1:n.221-25047G>T
ENST00000307046.8:c.221-25047G>T (IGF1)	ENSP00000302665.8:n.221-25047G>T
ENST00000337514.10:c.221-25047G>T (IGF1)	ENSP00000337612.6:n.221-25047G>T
ENST00000392904.5:c.221-25047G>T (IGF1)	ENSP00000376637.1:n.221-25047G>T
ENST00000392905.6:c.164-25047G>T (IGF1)	ENSP00000376638.2:n.164-25047G>T
ENST00000424202.6:c.173-25047G>T (IGF1)	ENSP00000416811.2:n.173-25047G>T
ENST00000456098.5:c.221-25047G>T (IGF1)	ENSP00000394999.1:n.221-25047G>T
NM_000618.3:c.221-25047G>T (IGF1)	NP_000609.1:n.221-25047G>T
NM_000618.4:c.221-25047G>T (IGF1)	NP_000609.1:n.221-25047G>T
NM_001111283.1:c.221-25047G>T (IGF1)	NP_001104753.1:n.221-25047G>T
NM_001111283.2:c.221-25047G>T (IGF1)	NP_001104753.1:n.221-25047G>T
NM_001111284.1:c.173-25047G>T (IGF1)	NP_001104754.1:n.173-25047G>T
NM_001111285.1:c.221-25047G>T (IGF1)	NP_001104755.1:n.221-25047G>T
XR_944534.1:n.480-25047G>T (IGF1)
XR_944535.1:n.257-25047G>T (IGF1)
XR_944536.1:n.242-25047G>T (IGF1)
XR_945270.1:n.6686-17991C>A (LINC02456)
XR_945271.1:n.5739-17991C>A (LINC02456)
XR_945272.1:n.6686-11050C>A (LINC02456)
XR_945273.1:n.6636-17991C>A (LINC02456)
XR_945274.1:n.6362-17991C>A (LINC02456)
XR_945275.1:n.6242-17991C>A (LINC02456)
XR_945276.1:n.6214-17991C>A (LINC02456)
XR_945277.1:n.2310-17991C>A (LINC02456)
NM_001111285.2:c.221-25047G>T (IGF1)	NP_001104755.1:n.221-25047G>T
XM_017019259.1:c.272-25047G>T (IGF1)	XP_016874748.1:n.272-25047G>T
XM_017019261.1:c.173-25047G>T (IGF1)	XP_016874750.1:n.173-25047G>T
XM_017019262.2:c.272-25047G>T (IGF1)	XP_016874751.1:n.272-25047G>T
XM_017019263.2:c.272-25047G>T (IGF1)	XP_016874752.1:n.272-25047G>T
XR_001749285.1:n.3135-17991C>A (LINC02456)
NM_000618.5:c.221-25047G>T (IGF1) MANE Select	NP_000609.1:n.221-25047G>T
NM_001111283.3:c.221-25047G>T (IGF1)	NP_001104753.1:n.221-25047G>T
NM_001111284.2:c.173-25047G>T (IGF1)	NP_001104754.1:n.173-25047G>T
NM_001111285.3:c.221-25047G>T (IGF1)	NP_001104755.1:n.221-25047G>T