Canonical Allele Identifier: CA1590297745

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148994600_148994632delinsATGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGT , CM000667.2:g.148994600_148994632delinsATGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGT	GRCh38
NC_000005.9:g.148374163_148374195delinsATGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGT , CM000667.1:g.148374163_148374195delinsATGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGT	GRCh37
NC_000005.8:g.148354356_148354388delinsATGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGT	NCBI36
NG_007947.2:g.73543_73575delinsACCAACCAACCAACCAACCAACCAACCAACCAT , LRG_269:g.73543_73575delinsACCAACCAACCAACCAACCAACCAACCAACCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000515425.6:c.*10079_*10111delinsACCAACCAACCAACCAACCAACCAACCAACCAT MANE Select	ENSP00000423660.1:n.*10079_*10111delinsAC...
ENST00000504690.5:c.*12+9094_*12+9126delinsACCAACCAACCAACCAACCAACCAACCAACCAT	ENSP00000425627.1:n.*12+9094_*12+9126deli...
ENST00000510350.1:n.231+12249_231+12281delinsACCAACCAACCAACCAACCAACCAACCAACCAT
NM_024577.3:c.*10079_*10111delinsACCAACCAACCAACCAACCAACCAACCAACCAT , LRG_269t1:c.*10079_*10111delinsACCAACCAACCAACCAACCAACCAACCAACCAT	NP_078853.2:n.*10079_*10111delinsACCAACCA...
NM_024577.4:c.*10079_*10111delinsACCAACCAACCAACCAACCAACCAACCAACCAT MANE Select	NP_078853.2:n.*10079_*10111delinsACCAACCA...