Canonical Allele Identifier: CA1590297811
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994652_148994655delinsTTGG , CM000667.2:g.148994652_148994655delinsTTGG GRCh38
NC_000005.9:g.148374215_148374218delinsTTGG , CM000667.1:g.148374215_148374218delinsTTGG GRCh37
NC_000005.8:g.148354408_148354411delinsTTGG NCBI36
NG_007947.2:g.73520_73523delinsCCAA , LRG_269:g.73520_73523delinsCCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000515425.6:c.*10056_*10059delinsCCAA MANE Select ENSP00000423660.1:n.*10056_*10059delinsCCAA
ENST00000504690.5:c.*12+9071_*12+9074delinsCCAA ENSP00000425627.1:n.*12+9071_*12+9074delinsCCAA
ENST00000510350.1:n.231+12226_231+12229delinsCCAA
NM_024577.3:c.*10056_*10059delinsCCAA , LRG_269t1:c.*10056_*10059delinsCCAA NP_078853.2:n.*10056_*10059delinsCCAA
NM_024577.4:c.*10056_*10059delinsCCAA MANE Select NP_078853.2:n.*10056_*10059delinsCCAA