Canonical Allele Identifier: CA1590297783
Gene: SH3TC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994629_148994630delinsTG , CM000667.2:g.148994629_148994630delinsTG GRCh38
NC_000005.9:g.148374192_148374193delinsTG , CM000667.1:g.148374192_148374193delinsTG GRCh37
NC_000005.8:g.148354385_148354386delinsTG NCBI36
NG_007947.2:g.73545_73546delinsCA , LRG_269:g.73545_73546delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10081_*10082delinsCA MANE Select ENSP00000423660.1:n.*10081_*10082delinsCA
ENST00000504690.5:c.*12+9096_*12+9097delinsCA ENSP00000425627.1:n.*12+9096_*12+9097delinsCA
ENST00000510350.1:n.231+12251_231+12252delinsCA
NM_024577.3:c.*10081_*10082delinsCA , LRG_269t1:c.*10081_*10082delinsCA NP_078853.2:n.*10081_*10082delinsCA
NM_024577.4:c.*10081_*10082delinsCA MANE Select NP_078853.2:n.*10081_*10082delinsCA
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