Canonical Allele Identifier: CA2580602097

Gene: IGF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102465050G>T , CM000674.2:g.102465050G>T	GRCh38
NC_000012.11:g.102858828G>T , CM000674.1:g.102858828G>T	GRCh37
NC_000012.10:g.101382958G>T	NCBI36
NG_011713.1:g.20551C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000337514.11:c.220+10593C>A MANE Select	ENSP00000337612.7:n.220+10593C>A
ENST00000392905.7:c.220+10593C>A	ENSP00000376638.3:n.220+10593C>A
ENST00000644491.1:c.220+10593C>A	ENSP00000494228.1:n.220+10593C>A
ENST00000307046.8:c.220+10593C>A	ENSP00000302665.8:n.220+10593C>A
ENST00000337514.10:c.220+10593C>A	ENSP00000337612.6:n.220+10593C>A
ENST00000392904.5:c.220+10593C>A	ENSP00000376637.1:n.220+10593C>A
ENST00000392905.6:c.163+10593C>A	ENSP00000376638.2:n.163+10593C>A
ENST00000424202.6:c.172+10593C>A	ENSP00000416811.2:n.172+10593C>A
ENST00000456098.5:c.220+10593C>A	ENSP00000394999.1:n.220+10593C>A
NM_000618.3:c.220+10593C>A	NP_000609.1:n.220+10593C>A
NM_000618.4:c.220+10593C>A	NP_000609.1:n.220+10593C>A
NM_001111283.1:c.220+10593C>A	NP_001104753.1:n.220+10593C>A
NM_001111283.2:c.220+10593C>A	NP_001104753.1:n.220+10593C>A
NM_001111284.1:c.172+10593C>A	NP_001104754.1:n.172+10593C>A
NM_001111285.1:c.220+10593C>A	NP_001104755.1:n.220+10593C>A
XR_944534.1:n.479+10593C>A
XR_944535.1:n.256+10593C>A
XR_944536.1:n.241+10593C>A
NM_001111285.2:c.220+10593C>A	NP_001104755.1:n.220+10593C>A
XM_017019259.1:c.271+10593C>A	XP_016874748.1:n.271+10593C>A
XM_017019261.1:c.172+10593C>A	XP_016874750.1:n.172+10593C>A
XM_017019262.2:c.271+10593C>A	XP_016874751.1:n.271+10593C>A
XM_017019263.2:c.271+10593C>A	XP_016874752.1:n.271+10593C>A
NM_000618.5:c.220+10593C>A MANE Select	NP_000609.1:n.220+10593C>A
NM_001111283.3:c.220+10593C>A	NP_001104753.1:n.220+10593C>A
NM_001111284.2:c.172+10593C>A	NP_001104754.1:n.172+10593C>A
NM_001111285.3:c.220+10593C>A	NP_001104755.1:n.220+10593C>A