Canonical Allele Identifier: CA2201869038

Gene: IGFALS SPSB3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1791006G= , CM000678.2:g.1791006G=	GRCh38
NC_000016.9:g.1841007G= , CM000678.1:g.1841007G=	GRCh37
NC_000016.8:g.1781008G=	NCBI36
NG_011778.1:g.7728C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215539.4:c.1412C= (IGFALS) MANE Select	ENSP00000215539.3:p.Ala471=
ENST00000215539.3:c.1412C= (IGFALS)	ENSP00000215539.3:p.Ala471=
ENST00000415638.3:c.1526C= (IGFALS)	ENSP00000416683.3:p.Ala509=
ENST00000569769.1:c.-13+2631C= (SPSB3)	ENSP00000455098.1:n.-13+2631C=
NM_001146006.1:c.1526C= (IGFALS)	NP_001139478.1:p.Ala509=
NM_004970.2:c.1412C= (IGFALS)	NP_004961.1:p.Ala471=
NR_027389.1:n.1466C= (IGFALS)
XM_011522476.1:c.1493C= (IGFALS)	XP_011520778.1:p.Ala498=
NM_001146006.2:c.1526C= (IGFALS)	NP_001139478.1:p.Ala509=
NM_004970.3:c.1412C= (IGFALS) MANE Select	NP_004961.1:p.Ala471=