Canonical Allele Identifier: CA1590297842
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994683_148994699delinsAATGGATGGATGGAAGG , CM000667.2:g.148994683_148994699delinsAATGGATGGATGGAAGG GRCh38
NC_000005.9:g.148374246_148374262delinsAATGGATGGATGGAAGG , CM000667.1:g.148374246_148374262delinsAATGGATGGATGGAAGG GRCh37
NC_000005.8:g.148354439_148354455delinsAATGGATGGATGGAAGG NCBI36
NG_007947.2:g.73476_73492delinsCCTTCCATCCATCCATT , LRG_269:g.73476_73492delinsCCTTCCATCCATCCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10012_*10028delinsCCTTCCATCCATCCATT MANE Select ENSP00000423660.1:n.*10012_*10028delinsCCTTCCATCCATCCATT
ENST00000504690.5:c.*12+9027_*12+9043delinsCCTTCCATCCATCCATT ENSP00000425627.1:n.*12+9027_*12+9043delinsCCTTCCATCCATCCATT
ENST00000510350.1:n.231+12182_231+12198delinsCCTTCCATCCATCCATT
NM_024577.3:c.*10012_*10028delinsCCTTCCATCCATCCATT , LRG_269t1:c.*10012_*10028delinsCCTTCCATCCATCCATT NP_078853.2:n.*10012_*10028delinsCCTTCCATCCATCCATT
NM_024577.4:c.*10012_*10028delinsCCTTCCATCCATCCATT MANE Select NP_078853.2:n.*10012_*10028delinsCCTTCCATCCATCCATT