Canonical Allele Identifier: CA2768852606
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994625_148994626del , CM000667.2:g.148994625_148994626del GRCh38
NC_000005.9:g.148374188_148374189del , CM000667.1:g.148374188_148374189del GRCh37
NC_000005.8:g.148354381_148354382del NCBI36
NG_007947.2:g.73549_73550del , LRG_269:g.73549_73550del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10085_*10086del MANE Select ENSP00000423660.1:n.*10085_*10086del
ENST00000504690.5:c.*12+9100_*12+9101del ENSP00000425627.1:n.*12+9100_*12+9101del
ENST00000510350.1:n.231+12255_231+12256del
NM_024577.3:c.*10085_*10086del , LRG_269t1:c.*10085_*10086del NP_078853.2:n.*10085_*10086del
NM_024577.4:c.*10085_*10086del MANE Select NP_078853.2:n.*10085_*10086del