Canonical Allele Identifier: CA2631055396

Gene: IGFALS SPSB3

Linked Data

• gnomAD v4: 16-1790940-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1790942del , CM000678.2:g.1790942del	GRCh38
NC_000016.9:g.1840943del , CM000678.1:g.1840943del	GRCh37
NC_000016.8:g.1780944del	NCBI36
NG_011778.1:g.7793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215539.4:c.1477del (IGFALS) MANE Select	ENSP00000215539.3:p.Arg493AlafsTer?
ENST00000215539.3:c.1477del (IGFALS)	ENSP00000215539.3:p.Arg493AlafsTer?
ENST00000415638.3:c.1591del (IGFALS)	ENSP00000416683.3:p.Arg531AlafsTer?
ENST00000569769.1:c.-13+2696del (SPSB3)	ENSP00000455098.1:n.-13+2696del
NM_001146006.1:c.1591del (IGFALS)	NP_001139478.1:p.Arg531AlafsTer?
NM_004970.2:c.1477del (IGFALS)	NP_004961.1:p.Arg493AlafsTer?
NR_027389.1:n.1531del (IGFALS)
XM_011522476.1:c.1558del (IGFALS)	XP_011520778.1:p.Arg520AlafsTer?
NM_001146006.2:c.1591del (IGFALS)	NP_001139478.1:p.Arg531AlafsTer?
NM_004970.3:c.1477del (IGFALS) MANE Select	NP_004961.1:p.Arg493AlafsTer?