Canonical Allele Identifier: CA1590297740
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994598_148994608delinsAGATGGTTGGT , CM000667.2:g.148994598_148994608delinsAGATGGTTGGT GRCh38
NC_000005.9:g.148374161_148374171delinsAGATGGTTGGT , CM000667.1:g.148374161_148374171delinsAGATGGTTGGT GRCh37
NC_000005.8:g.148354354_148354364delinsAGATGGTTGGT NCBI36
NG_007947.2:g.73567_73577delinsACCAACCATCT , LRG_269:g.73567_73577delinsACCAACCATCT

Transcript Alleles

HGVS Amino-acid change
ENST00000515425.6:c.*10103_*10113delinsACCAACCATCT MANE Select ENSP00000423660.1:n.*10103_*10113delinsAC...
ENST00000504690.5:c.*12+9118_*12+9128delinsACCAACCATCT ENSP00000425627.1:n.*12+9118_*12+9128deli...
ENST00000510350.1:n.231+12273_231+12283delinsACCAACCATCT
NM_024577.3:c.*10103_*10113delinsACCAACCATCT , LRG_269t1:c.*10103_*10113delinsACCAACCATCT NP_078853.2:n.*10103_*10113delinsACCAACCA...
NM_024577.4:c.*10103_*10113delinsACCAACCATCT MANE Select NP_078853.2:n.*10103_*10113delinsACCAACCA...