Canonical Allele Identifier: CA2201869049

Gene: IGFALS SPSB3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1791012C= , CM000678.2:g.1791012C=	GRCh38
NC_000016.9:g.1841013C= , CM000678.1:g.1841013C=	GRCh37
NC_000016.8:g.1781014C=	NCBI36
NG_011778.1:g.7722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215539.4:c.1406G= (IGFALS) MANE Select	ENSP00000215539.3:p.Arg469=
ENST00000215539.3:c.1406G= (IGFALS)	ENSP00000215539.3:p.Arg469=
ENST00000415638.3:c.1520G= (IGFALS)	ENSP00000416683.3:p.Arg507=
ENST00000569769.1:c.-13+2625G= (SPSB3)	ENSP00000455098.1:n.-13+2625G=
NM_001146006.1:c.1520G= (IGFALS)	NP_001139478.1:p.Arg507=
NM_004970.2:c.1406G= (IGFALS)	NP_004961.1:p.Arg469=
NR_027389.1:n.1460G= (IGFALS)
XM_011522476.1:c.1487G= (IGFALS)	XP_011520778.1:p.Arg496=
NM_001146006.2:c.1520G= (IGFALS)	NP_001139478.1:p.Arg507=
NM_004970.3:c.1406G= (IGFALS) MANE Select	NP_004961.1:p.Arg469=