Canonical Allele Identifier: CA638940767
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs1305628965
gnomAD v2: 22-20780098-C-CA
MyVariant Identifiers: chr22:g.20780098_20780099insA (hg19) chr22:g.20425811_20425812insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425811_20425812insA , CM000684.2:g.20425811_20425812insA GRCh38
NC_000022.10:g.20780098_20780099insA , CM000684.1:g.20780098_20780099insA GRCh37
NC_000022.9:g.19110098_19110099insA NCBI36
NG_031868.2:g.17048_17049insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2164_2165insT MANE Select ENSP00000477564.2:p.Arg722LeufsTer?
ENST00000615031.4:c.2179_2180insT ENSP00000479389.1:p.Arg727LeufsTer?
ENST00000622235.4:c.2164_2165insT ENSP00000477564.1:p.Arg722LeufsTer?
ENST00000623402.1:c.2179_2180insT ENSP00000485276.1:p.Arg727LeufsTer?
NM_153334.6:c.2179_2180insT NP_699165.3:p.Arg727LeufsTer?
NM_182895.4:c.2164_2165insT NP_878315.2:p.Arg722LeufsTer?
NM_153334.7:c.2179_2180insT NP_699165.3:p.Arg727LeufsTer?
NM_182895.5:c.2164_2165insT MANE Select NP_878315.2:p.Arg722LeufsTer?
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