Canonical Allele Identifier: CA394263770

Gene: IGFALS SPSB3

Linked Data

• dbSNP Id: rs1897203532
• gnomAD v3: 16-1790835-A-G
• gnomAD v4: 16-1790835-A-G
• MyVariant Identifiers: chr16:g.1840836A>G (hg19) ; chr16:g.1790835A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1790835A>G , CM000678.2:g.1790835A>G	GRCh38
NC_000016.9:g.1840836A>G , CM000678.1:g.1840836A>G	GRCh37
NC_000016.8:g.1780837A>G	NCBI36
NG_011778.1:g.7899T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215539.4:c.1583T>C (IGFALS) MANE Select	ENSP00000215539.3:p.Leu528Pro
ENST00000215539.3:c.1583T>C (IGFALS)	ENSP00000215539.3:p.Leu528Pro
ENST00000415638.3:c.1697T>C (IGFALS)	ENSP00000416683.3:p.Leu566Pro
ENST00000569769.1:c.-13+2802T>C (SPSB3)	ENSP00000455098.1:n.-13+2802T>C
NM_001146006.1:c.1697T>C (IGFALS)	NP_001139478.1:p.Leu566Pro
NM_004970.2:c.1583T>C (IGFALS)	NP_004961.1:p.Leu528Pro
NR_027389.1:n.1637T>C (IGFALS)
XM_011522476.1:c.1664T>C (IGFALS)	XP_011520778.1:p.Leu555Pro
NM_001146006.2:c.1697T>C (IGFALS)	NP_001139478.1:p.Leu566Pro
NM_004970.3:c.1583T>C (IGFALS) MANE Select	NP_004961.1:p.Leu528Pro