Canonical Allele Identifier: CA394263839
Gene: IGFALS HGNC NCBI
SPSB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1790856A>T , CM000678.2:g.1790856A>T GRCh38
NC_000016.9:g.1840857A>T , CM000678.1:g.1840857A>T GRCh37
NC_000016.8:g.1780858A>T NCBI36
NG_011778.1:g.7878T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215539.4:c.1562T>A (IGFALS) MANE Select ENSP00000215539.3:p.Phe521Tyr
ENST00000215539.3:c.1562T>A (IGFALS) ENSP00000215539.3:p.Phe521Tyr
ENST00000415638.3:c.1676T>A (IGFALS) ENSP00000416683.3:p.Phe559Tyr
ENST00000569769.1:c.-13+2781T>A (SPSB3) ENSP00000455098.1:n.-13+2781T>A
NM_001146006.1:c.1676T>A (IGFALS) NP_001139478.1:p.Phe559Tyr
NM_004970.2:c.1562T>A (IGFALS) NP_004961.1:p.Phe521Tyr
NR_027389.1:n.1616T>A (IGFALS)
XM_011522476.1:c.1643T>A (IGFALS) XP_011520778.1:p.Phe548Tyr
NM_001146006.2:c.1676T>A (IGFALS) NP_001139478.1:p.Phe559Tyr
NM_004970.3:c.1562T>A (IGFALS) MANE Select NP_004961.1:p.Phe521Tyr