Canonical Allele Identifier: CA2497029646
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994600_148994604delinsATGGT , CM000667.2:g.148994600_148994604delinsATGGT GRCh38
NC_000005.9:g.148374163_148374167delinsATGGT , CM000667.1:g.148374163_148374167delinsATGGT GRCh37
NC_000005.8:g.148354356_148354360delinsATGGT NCBI36
NG_007947.2:g.73571_73575delinsACCAT , LRG_269:g.73571_73575delinsACCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000515425.6:c.*10107_*10111delinsACCAT MANE Select ENSP00000423660.1:n.*10107_*10111delinsACCAT
ENST00000504690.5:c.*12+9122_*12+9126delinsACCAT ENSP00000425627.1:n.*12+9122_*12+9126delinsACCAT
ENST00000510350.1:n.231+12277_231+12281delinsACCAT
NM_024577.3:c.*10107_*10111delinsACCAT , LRG_269t1:c.*10107_*10111delinsACCAT NP_078853.2:n.*10107_*10111delinsACCAT
NM_024577.4:c.*10107_*10111delinsACCAT MANE Select NP_078853.2:n.*10107_*10111delinsACCAT