Canonical Allele Identifier: CA10631912
Gene: IGF1 HGNC NCBI
LINC02456 HGNC NCBI

Linked Data

ClinVar Variation Id: 306830
ClinVar RCV Id: RCV000391004
dbSNP Id: rs5742714
gnomAD v2: 12-102789852-C-G
gnomAD v3: 12-102396074-C-G
gnomAD v4: 12-102396074-C-G
MyVariant Identifiers: chr12:g.102789852C>G (hg19) chr12:g.102396074C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102396074C>G , CM000674.2:g.102396074C>G GRCh38
NC_000012.11:g.102789852C>G , CM000674.1:g.102789852C>G GRCh37
NC_000012.10:g.101313982C>G NCBI36
NG_011713.1:g.89527G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000337514.11:c.*6433G>C (IGF1) MANE Select ENSP00000337612.7:n.*6433G>C
ENST00000337514.10:c.*6433G>C (IGF1) ENSP00000337612.6:n.*6433G>C
ENST00000456098.5:c.*6467G>C (IGF1) ENSP00000394999.1:n.*6467G>C
NM_000618.3:c.*6433G>C (IGF1) NP_000609.1:n.*6433G>C
NM_000618.4:c.*6433G>C (IGF1) NP_000609.1:n.*6433G>C
NM_001111283.1:c.*6467G>C (IGF1) NP_001104753.1:n.*6467G>C
NM_001111283.2:c.*6467G>C (IGF1) NP_001104753.1:n.*6467G>C
NM_001111284.1:c.*6433G>C (IGF1) NP_001104754.1:n.*6433G>C
XR_945270.1:n.582-8039C>G (LINC02456)
XR_945271.1:n.582-8039C>G (LINC02456)
XR_945272.1:n.582-8039C>G (LINC02456)
XR_945273.1:n.532-8039C>G (LINC02456)
XR_945274.1:n.258-8039C>G (LINC02456)
XR_945275.1:n.138-8039C>G (LINC02456)
XR_945276.1:n.110-8039C>G (LINC02456)
XR_945277.1:n.582-8039C>G (LINC02456)
XM_017019262.2:c.*6467G>C (IGF1) XP_016874751.1:n.*6467G>C
XM_017019263.2:c.*6433G>C (IGF1) XP_016874752.1:n.*6433G>C
XR_001749285.1:n.697-8039C>G (LINC02456)
XR_001749286.1:n.258-8039C>G (LINC02456)
XR_001749287.1:n.576-8039C>G (LINC02456)
XR_001749288.1:n.1585-8039C>G (LINC02456)
NM_000618.5:c.*6433G>C (IGF1) MANE Select NP_000609.1:n.*6433G>C
NM_001111283.3:c.*6467G>C (IGF1) NP_001104753.1:n.*6467G>C
NM_001111284.2:c.*6433G>C (IGF1) NP_001104754.1:n.*6433G>C
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