Canonical Allele Identifier: CA1590297802
Gene: SH3TC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994645_148994646delinsTG , CM000667.2:g.148994645_148994646delinsTG GRCh38
NC_000005.9:g.148374208_148374209delinsTG , CM000667.1:g.148374208_148374209delinsTG GRCh37
NC_000005.8:g.148354401_148354402delinsTG NCBI36
NG_007947.2:g.73529_73530delinsCA , LRG_269:g.73529_73530delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10065_*10066delinsCA MANE Select ENSP00000423660.1:n.*10065_*10066delinsCA
ENST00000504690.5:c.*12+9080_*12+9081delinsCA ENSP00000425627.1:n.*12+9080_*12+9081delinsCA
ENST00000510350.1:n.231+12235_231+12236delinsCA
NM_024577.3:c.*10065_*10066delinsCA , LRG_269t1:c.*10065_*10066delinsCA NP_078853.2:n.*10065_*10066delinsCA
NM_024577.4:c.*10065_*10066delinsCA MANE Select NP_078853.2:n.*10065_*10066delinsCA
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