Canonical Allele Identifier: CA1590303401
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149007047T= , CM000667.2:g.149007047T= GRCh38
NC_000005.9:g.148386610T= , CM000667.1:g.148386610T= GRCh37
NC_000005.8:g.148366803T= NCBI36
NG_007947.2:g.61128A= , LRG_269:g.61128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502274.2:c.4362A=
ENST00000515425.6:c.3509A= MANE Select ENSP00000423660.1:p.His1170=
ENST00000675793.1:c.*4566A= ENSP00000502039.1:n.*4566A=
ENST00000323829.9:c.*2897A= ENSP00000313025.5:n.*2897A=
ENST00000502274.1:c.95A= ENSP00000421092.1:p.His32=
ENST00000504517.5:c.3031A= ENSP00000421779.1:n.3031A=
ENST00000504690.5:c.3509A= ENSP00000425627.1:p.His1170=
ENST00000510350.1:n.65A=
ENST00000510779.1:c.2559A=
ENST00000512049.5:c.3488A= ENSP00000421860.1:p.His1163=
ENST00000515229.5:n.171A=
ENST00000515425.5:c.3509A= ENSP00000423660.1:p.His1170=
NM_024577.3:c.3509A= , LRG_269t1:c.3509A= NP_078853.2:p.His1170=
NM_024577.4:c.3509A= MANE Select NP_078853.2:p.His1170=