Canonical Allele Identifier: CA650763944
Gene: SH3TC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994599_148994600insTGGT , CM000667.2:g.148994599_148994600insTGGT GRCh38
NC_000005.9:g.148374162_148374163insTGGT , CM000667.1:g.148374162_148374163insTGGT GRCh37
NC_000005.8:g.148354355_148354356insTGGT NCBI36
NG_007947.2:g.73575_73576insACCA , LRG_269:g.73575_73576insACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10111_*10112insACCA MANE Select ENSP00000423660.1:n.*10111_*10112insACCA
ENST00000504690.5:c.*12+9126_*12+9127insACCA ENSP00000425627.1:n.*12+9126_*12+9127insACCA
ENST00000510350.1:n.231+12281_231+12282insACCA
NM_024577.3:c.*10111_*10112insACCA , LRG_269t1:c.*10111_*10112insACCA NP_078853.2:n.*10111_*10112insACCA
NM_024577.4:c.*10111_*10112insACCA MANE Select NP_078853.2:n.*10111_*10112insACCA