Canonical Allele Identifier: CA1590303405
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149007054C= , CM000667.2:g.149007054C= GRCh38
NC_000005.9:g.148386617C= , CM000667.1:g.148386617C= GRCh37
NC_000005.8:g.148366810C= NCBI36
NG_007947.2:g.61121G= , LRG_269:g.61121G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502274.2:c.4355G=
ENST00000515425.6:c.3502G= MANE Select ENSP00000423660.1:p.Ala1168=
ENST00000675793.1:c.*4559G= ENSP00000502039.1:n.*4559G=
ENST00000323829.9:c.*2890G= ENSP00000313025.5:n.*2890G=
ENST00000502274.1:c.88G= ENSP00000421092.1:p.Ala30=
ENST00000504517.5:c.3024G= ENSP00000421779.1:n.3024G=
ENST00000504690.5:c.3502G= ENSP00000425627.1:p.Ala1168=
ENST00000510350.1:n.58G=
ENST00000510779.1:c.2552G=
ENST00000512049.5:c.3481G= ENSP00000421860.1:p.Ala1161=
ENST00000515229.5:n.164G=
ENST00000515425.5:c.3502G= ENSP00000423660.1:p.Ala1168=
NM_024577.3:c.3502G= , LRG_269t1:c.3502G= NP_078853.2:p.Ala1168=
NM_024577.4:c.3502G= MANE Select NP_078853.2:p.Ala1168=