Canonical Allele Identifier: CA2631055358
Gene: IGFALS HGNC NCBI
SPSB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1790926dup , CM000678.2:g.1790926dup GRCh38
NC_000016.9:g.1840927dup , CM000678.1:g.1840927dup GRCh37
NC_000016.8:g.1780928dup NCBI36
NG_011778.1:g.7810dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215539.4:c.1494dup (IGFALS) MANE Select ENSP00000215539.3:p.Asn499GlnfsTer?
ENST00000215539.3:c.1494dup (IGFALS) ENSP00000215539.3:p.Asn499GlnfsTer?
ENST00000415638.3:c.1608dup (IGFALS) ENSP00000416683.3:p.Asn537GlnfsTer?
ENST00000569769.1:c.-13+2713dup (SPSB3) ENSP00000455098.1:n.-13+2713dup
NM_001146006.1:c.1608dup (IGFALS) NP_001139478.1:p.Asn537GlnfsTer?
NM_004970.2:c.1494dup (IGFALS) NP_004961.1:p.Asn499GlnfsTer?
NR_027389.1:n.1548dup (IGFALS)
XM_011522476.1:c.1575dup (IGFALS) XP_011520778.1:p.Asn526GlnfsTer?
NM_001146006.2:c.1608dup (IGFALS) NP_001139478.1:p.Asn537GlnfsTer?
NM_004970.3:c.1494dup (IGFALS) MANE Select NP_004961.1:p.Asn499GlnfsTer?