Canonical Allele Identifier: CA1590297732
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994592_148994600delinsGTGGTTAGA , CM000667.2:g.148994592_148994600delinsGTGGTTAGA GRCh38
NC_000005.9:g.148374155_148374163delinsGTGGTTAGA , CM000667.1:g.148374155_148374163delinsGTGGTTAGA GRCh37
NC_000005.8:g.148354348_148354356delinsGTGGTTAGA NCBI36
NG_007947.2:g.73575_73583delinsTCTAACCAC , LRG_269:g.73575_73583delinsTCTAACCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10111_*10119delinsTCTAACCAC MANE Select ENSP00000423660.1:n.*10111_*10119delinsTCTAACCAC
ENST00000504690.5:c.*12+9126_*12+9134delinsTCTAACCAC ENSP00000425627.1:n.*12+9126_*12+9134delinsTCTAACCAC
ENST00000510350.1:n.231+12281_231+12289delinsTCTAACCAC
NM_024577.3:c.*10111_*10119delinsTCTAACCAC , LRG_269t1:c.*10111_*10119delinsTCTAACCAC NP_078853.2:n.*10111_*10119delinsTCTAACCAC
NM_024577.4:c.*10111_*10119delinsTCTAACCAC MANE Select NP_078853.2:n.*10111_*10119delinsTCTAACCAC