Canonical Allele Identifier: CA513694898
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs1555907075
MyVariant Identifiers: chr22:g.20779976del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425687del , CM000684.2:g.20425687del GRCh38
NC_000022.10:g.20779976del , CM000684.1:g.20779976del GRCh37
NC_000022.9:g.19109976del NCBI36
NG_031868.2:g.17173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2289del MANE Select ENSP00000477564.2:p.Glu765ArgfsTer?
ENST00000615031.4:c.2302del ENSP00000479389.1:p.Ala768ProfsTer?
ENST00000622235.4:c.2289del ENSP00000477564.1:p.Glu765ArgfsTer?
ENST00000623402.1:c.2304del ENSP00000485276.1:p.Glu770ArgfsTer?
NM_153334.6:c.2304del NP_699165.3:p.Glu770ArgfsTer?
NM_182895.4:c.2289del NP_878315.2:p.Glu765ArgfsTer?
NM_153334.7:c.2304del NP_699165.3:p.Glu770ArgfsTer?
NM_182895.5:c.2289del MANE Select NP_878315.2:p.Glu765ArgfsTer?