Canonical Allele Identifier: CA2201868711
Gene: IGFALS HGNC NCBI
SPSB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1790850G= , CM000678.2:g.1790850G= GRCh38
NC_000016.9:g.1840851G= , CM000678.1:g.1840851G= GRCh37
NC_000016.8:g.1780852G= NCBI36
NG_011778.1:g.7884C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215539.4:c.1568C= (IGFALS) MANE Select ENSP00000215539.3:p.Pro523=
ENST00000215539.3:c.1568C= (IGFALS) ENSP00000215539.3:p.Pro523=
ENST00000415638.3:c.1682C= (IGFALS) ENSP00000416683.3:p.Pro561=
ENST00000569769.1:c.-13+2787C= (SPSB3) ENSP00000455098.1:n.-13+2787C=
NM_001146006.1:c.1682C= (IGFALS) NP_001139478.1:p.Pro561=
NM_004970.2:c.1568C= (IGFALS) NP_004961.1:p.Pro523=
NR_027389.1:n.1622C= (IGFALS)
XM_011522476.1:c.1649C= (IGFALS) XP_011520778.1:p.Pro550=
NM_001146006.2:c.1682C= (IGFALS) NP_001139478.1:p.Pro561=
NM_004970.3:c.1568C= (IGFALS) MANE Select NP_004961.1:p.Pro523=