Canonical Allele Identifier: CA638940761
Gene: SCARF2 HGNC NCBI

Linked Data

gnomAD v2: 22-20779973-C-CT
MyVariant Identifiers: chr22:g.20779973_20779974insT (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425684_20425685insT , CM000684.2:g.20425684_20425685insT GRCh38
NC_000022.10:g.20779973_20779974insT , CM000684.1:g.20779973_20779974insT GRCh37
NC_000022.9:g.19109973_19109974insT NCBI36
NG_031868.2:g.17175_17176insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2291_2292insA MANE Select ENSP00000477564.2:p.Glu765ArgfsTer9
ENST00000615031.4:c.2304_2305-1insA ENSP00000479389.1:n.2304_2305-1insA
ENST00000622235.4:c.2291_2292insA ENSP00000477564.1:p.Glu765ArgfsTer9
ENST00000623402.1:c.2306_2307insA ENSP00000485276.1:p.Glu770ArgfsTer9
NM_153334.6:c.2306_2307insA NP_699165.3:p.Glu770ArgfsTer9
NM_182895.4:c.2291_2292insA NP_878315.2:p.Glu765ArgfsTer9
NM_153334.7:c.2306_2307insA NP_699165.3:p.Glu770ArgfsTer9
NM_182895.5:c.2291_2292insA MANE Select NP_878315.2:p.Glu765ArgfsTer9
Search 100 bp 5'
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