Canonical Allele Identifier: CA10112147
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs773838754
ExAC: 22:20779744 GTCT / G
gnomAD v2: 22-20779744-GTCT-G
gnomAD v3: 22-20425454-GTCT-G
gnomAD v4: 22-20425454-GTCT-G
MyVariant Identifiers: chr22:g.20779745_20779747del (hg19) chr22:g.20425455_20425457del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425460_20425462del , CM000684.2:g.20425460_20425462del GRCh38
NC_000022.10:g.20779750_20779752del , CM000684.1:g.20779750_20779752del GRCh37
NC_000022.9:g.19109750_19109752del NCBI36
NG_031868.2:g.17403_17405del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2519_2521del MANE Select ENSP00000477564.2:p.Lys840del
ENST00000615031.4:c.2531_2533del ENSP00000479389.1:p.Lys844del
ENST00000622235.4:c.2519_2521del ENSP00000477564.1:p.Lys840del
ENST00000623402.1:c.2534_2536del ENSP00000485276.1:p.Lys845del
NM_153334.6:c.2534_2536del NP_699165.3:p.Lys845del
NM_182895.4:c.2519_2521del NP_878315.2:p.Lys840del
NM_153334.7:c.2534_2536del NP_699165.3:p.Lys845del
NM_182895.5:c.2519_2521del MANE Select NP_878315.2:p.Lys840del
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