Canonical Allele Identifier: CA7820233

Gene: IGFALS SPSB3

Linked Data

• dbSNP Id: rs763718123
• ExAC: 16:1840712 G / A
• gnomAD v2: 16-1840712-G-A
• gnomAD v4: 16-1790711-G-A
• MyVariant Identifiers: chr16:g.1840712G>A (hg19) ; chr16:g.1790711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1790711G>A , CM000678.2:g.1790711G>A	GRCh38
NC_000016.9:g.1840712G>A , CM000678.1:g.1840712G>A	GRCh37
NC_000016.8:g.1780713G>A	NCBI36
NG_011778.1:g.8023C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000215539.4:c.1707C>T (IGFALS) MANE Select	ENSP00000215539.3:p.Asp569=
ENST00000215539.3:c.1707C>T (IGFALS)	ENSP00000215539.3:p.Asp569=
ENST00000415638.3:c.1821C>T (IGFALS)	ENSP00000416683.3:p.Asp607=
ENST00000569769.1:c.-13+2926C>T (SPSB3)	ENSP00000455098.1:n.-13+2926C>T
NM_001146006.1:c.1821C>T (IGFALS)	NP_001139478.1:p.Asp607=
NM_004970.2:c.1707C>T (IGFALS)	NP_004961.1:p.Asp569=
NR_027389.1:n.1761C>T (IGFALS)
XM_011522476.1:c.1788C>T (IGFALS)	XP_011520778.1:p.Asp596=
NM_001146006.2:c.1821C>T (IGFALS)	NP_001139478.1:p.Asp607=
NM_004970.3:c.1707C>T (IGFALS) MANE Select	NP_004961.1:p.Asp569=