Canonical Allele Identifier: CA2396362743
Gene: SCARF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425751_20425778delinsCGGGCCCTGGGCGGCGAGGGCGCAGCGA , CM000684.2:g.20425751_20425778delinsCGGGCCCTGGGCGGCGAGGGCGCAGCGA GRCh38
NC_000022.10:g.20780038_20780065delinsCGGGCCCTGGGCGGCGAGGGCGCAGCGA , CM000684.1:g.20780038_20780065delinsCGGGCCCTGGGCGGCGAGGGCGCAGCGA GRCh37
NC_000022.9:g.19110038_19110065delinsCGGGCCCTGGGCGGCGAGGGCGCAGCGA NCBI36
NG_031868.2:g.17082_17109delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2198_2225delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG MANE Select ENSP00000477564.2:p.Leu733=
ENST00000615031.4:c.2213_2240delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG ENSP00000479389.1:p.Leu738=
ENST00000622235.4:c.2198_2225delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG ENSP00000477564.1:p.Leu733=
ENST00000623402.1:c.2213_2240delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG ENSP00000485276.1:p.Leu738=
NM_153334.6:c.2213_2240delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG NP_699165.3:p.Leu738=
NM_182895.4:c.2198_2225delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG NP_878315.2:p.Leu733=
NM_153334.7:c.2213_2240delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG NP_699165.3:p.Leu738=
NM_182895.5:c.2198_2225delinsTCGCTGCGCCCTCGCCGCCCAGGGCCCG MANE Select NP_878315.2:p.Leu733=