Canonical Allele Identifier: CA276742686

Gene: IGFALS SPSB3

Linked Data

• dbSNP Id: rs144587967
• MyVariant Identifiers: chr16:g.1840814_1840815insC (hg19) ; chr16:g.1790813_1790814insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1790816dup , CM000678.2:g.1790816dup	GRCh38
NC_000016.9:g.1840817dup , CM000678.1:g.1840817dup	GRCh37
NC_000016.8:g.1780818dup	NCBI36
NG_011778.1:g.7920dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215539.4:c.1604dup (IGFALS) MANE Select	ENSP00000215539.3:p.Asn536Ter
ENST00000215539.3:c.1604dup (IGFALS)	ENSP00000215539.3:p.Asn536Ter
ENST00000415638.3:c.1718dup (IGFALS)	ENSP00000416683.3:p.Asn574Ter
ENST00000569769.1:c.-13+2823dup (SPSB3)	ENSP00000455098.1:n.-13+2823dup
NM_001146006.1:c.1718dup (IGFALS)	NP_001139478.1:p.Asn574Ter
NM_004970.2:c.1604dup (IGFALS)	NP_004961.1:p.Asn536Ter
NR_027389.1:n.1658dup (IGFALS)
XM_011522476.1:c.1685dup (IGFALS)	XP_011520778.1:p.Asn563Ter
NM_001146006.2:c.1718dup (IGFALS)	NP_001139478.1:p.Asn574Ter
NM_004970.3:c.1604dup (IGFALS) MANE Select	NP_004961.1:p.Asn536Ter