Canonical Allele Identifier: CA638940758
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs1569104788
MyVariant Identifiers: chr22:g.20779816del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425530del , CM000684.2:g.20425530del GRCh38
NC_000022.10:g.20779820del , CM000684.1:g.20779820del GRCh37
NC_000022.9:g.19109820del NCBI36
NG_031868.2:g.17334del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2450del MANE Select ENSP00000477564.2:p.Pro817GlnfsTer?
ENST00000615031.4:c.2462del ENSP00000479389.1:p.Pro821GlnfsTer?
ENST00000622235.4:c.2450del ENSP00000477564.1:p.Pro817GlnfsTer?
ENST00000623402.1:c.2465del ENSP00000485276.1:p.Pro822GlnfsTer?
NM_153334.6:c.2465del NP_699165.3:p.Pro822GlnfsTer?
NM_182895.4:c.2450del NP_878315.2:p.Pro817GlnfsTer?
NM_153334.7:c.2465del NP_699165.3:p.Pro822GlnfsTer?
NM_182895.5:c.2450del MANE Select NP_878315.2:p.Pro817GlnfsTer?