Canonical Allele Identifier: CA493035596

Gene: IGFALS SPSB3

Linked Data

• MyVariant Identifiers: chr16:g.1841006T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1791005T>C , CM000678.2:g.1791005T>C	GRCh38
NC_000016.9:g.1841006T>C , CM000678.1:g.1841006T>C	GRCh37
NC_000016.8:g.1781007T>C	NCBI36
NG_011778.1:g.7729A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215539.4:c.1413A>G (IGFALS) MANE Select	ENSP00000215539.3:p.Ala471=
ENST00000215539.3:c.1413A>G (IGFALS)	ENSP00000215539.3:p.Ala471=
ENST00000415638.3:c.1527A>G (IGFALS)	ENSP00000416683.3:p.Ala509=
ENST00000569769.1:c.-13+2632A>G (SPSB3)	ENSP00000455098.1:n.-13+2632A>G
NM_001146006.1:c.1527A>G (IGFALS)	NP_001139478.1:p.Ala509=
NM_004970.2:c.1413A>G (IGFALS)	NP_004961.1:p.Ala471=
NR_027389.1:n.1467A>G (IGFALS)
XM_011522476.1:c.1494A>G (IGFALS)	XP_011520778.1:p.Ala498=
NM_001146006.2:c.1527A>G (IGFALS)	NP_001139478.1:p.Ala509=
NM_004970.3:c.1413A>G (IGFALS) MANE Select	NP_004961.1:p.Ala471=