Canonical Allele Identifier: CA394264294
Gene: IGFALS HGNC NCBI
SPSB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1791034A>C , CM000678.2:g.1791034A>C GRCh38
NC_000016.9:g.1841035A>C , CM000678.1:g.1841035A>C GRCh37
NC_000016.8:g.1781036A>C NCBI36
NG_011778.1:g.7700T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215539.4:c.1384T>G (IGFALS) MANE Select ENSP00000215539.3:p.Tyr462Asp
ENST00000215539.3:c.1384T>G (IGFALS) ENSP00000215539.3:p.Tyr462Asp
ENST00000415638.3:c.1498T>G (IGFALS) ENSP00000416683.3:p.Tyr500Asp
ENST00000569769.1:c.-13+2603T>G (SPSB3) ENSP00000455098.1:n.-13+2603T>G
NM_001146006.1:c.1498T>G (IGFALS) NP_001139478.1:p.Tyr500Asp
NM_004970.2:c.1384T>G (IGFALS) NP_004961.1:p.Tyr462Asp
NR_027389.1:n.1438T>G (IGFALS)
XM_011522476.1:c.1465T>G (IGFALS) XP_011520778.1:p.Tyr489Asp
NM_001146006.2:c.1498T>G (IGFALS) NP_001139478.1:p.Tyr500Asp
NM_004970.3:c.1384T>G (IGFALS) MANE Select NP_004961.1:p.Tyr462Asp