Canonical Allele Identifier: CA1590297719
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994583_148994597delinsGGTGGTTGGGTGGTT , CM000667.2:g.148994583_148994597delinsGGTGGTTGGGTGGTT GRCh38
NC_000005.9:g.148374146_148374160delinsGGTGGTTGGGTGGTT , CM000667.1:g.148374146_148374160delinsGGTGGTTGGGTGGTT GRCh37
NC_000005.8:g.148354339_148354353delinsGGTGGTTGGGTGGTT NCBI36
NG_007947.2:g.73578_73592delinsAACCACCCAACCACC , LRG_269:g.73578_73592delinsAACCACCCAACCACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10114_*10128delinsAACCACCCAACCACC MANE Select ENSP00000423660.1:n.*10114_*10128delinsAACCACCCAACCACC
ENST00000504690.5:c.*12+9129_*12+9143delinsAACCACCCAACCACC ENSP00000425627.1:n.*12+9129_*12+9143delinsAACCACCCAACCACC
ENST00000510350.1:n.231+12284_231+12298delinsAACCACCCAACCACC
NM_024577.3:c.*10114_*10128delinsAACCACCCAACCACC , LRG_269t1:c.*10114_*10128delinsAACCACCCAACCACC NP_078853.2:n.*10114_*10128delinsAACCACCCAACCACC
NM_024577.4:c.*10114_*10128delinsAACCACCCAACCACC MANE Select NP_078853.2:n.*10114_*10128delinsAACCACCCAACCACC