Canonical Allele Identifier: CA16621827
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425358
dbSNP Id: rs1064797314

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149027836del , CM000667.2:g.149027836del GRCh38
NC_000005.9:g.148407399del , CM000667.1:g.148407399del GRCh37
NC_000005.8:g.148387592del NCBI36
NG_007947.2:g.40340del , LRG_269:g.40340del

Transcript Alleles

HGVS Amino-acid change
ENST00000502274.2:c.1793del
ENST00000515425.6:c.1897del MANE Select ENSP00000423660.1:p.Ala633ProfsTer12
ENST00000675793.1:c.*1181del ENSP00000502039.1:n.*1181del
ENST00000676056.1:c.*1407del ENSP00000501827.1:n.*1407del
ENST00000323829.9:c.*1285del ENSP00000313025.5:n.*1285del
ENST00000504517.5:c.1427del ENSP00000421779.1:n.1427del
ENST00000504690.5:c.1897del ENSP00000425627.1:p.Ala633ProfsTer12
ENST00000510779.1:c.947del
ENST00000511307.5:c.*1677del ENSP00000421420.1:n.*1677del
ENST00000512049.5:c.1876del ENSP00000421860.1:p.Ala626ProfsTer12
ENST00000513604.5:c.*1285del ENSP00000423111.1:n.*1285del
ENST00000515425.5:c.1897del ENSP00000423660.1:p.Ala633ProfsTer12
NM_024577.3:c.1897del , LRG_269t1:c.1897del NP_078853.2:p.Ala633ProfsTer12
NM_024577.4:c.1897del MANE Select NP_078853.2:p.Ala633ProfsTer12