Canonical Allele Identifier: CA1590303360
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149006954T= , CM000667.2:g.149006954T= GRCh38
NC_000005.9:g.148386517T= , CM000667.1:g.148386517T= GRCh37
NC_000005.8:g.148366710T= NCBI36
NG_007947.2:g.61221A= , LRG_269:g.61221A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502274.2:c.4455A=
ENST00000515425.6:c.3602A= MANE Select ENSP00000423660.1:p.Gln1201=
ENST00000675793.1:c.*4659A= ENSP00000502039.1:n.*4659A=
ENST00000323829.9:c.*2990A= ENSP00000313025.5:n.*2990A=
ENST00000502274.1:c.188A= ENSP00000421092.1:p.Gln63=
ENST00000504517.5:c.3124A= ENSP00000421779.1:n.3124A=
ENST00000504690.5:c.3602A= ENSP00000425627.1:p.Gln1201=
ENST00000510350.1:n.158A=
ENST00000510779.1:c.2652A=
ENST00000512049.5:c.3581A= ENSP00000421860.1:p.Gln1194=
ENST00000515229.5:n.264A=
ENST00000515425.5:c.3602A= ENSP00000423660.1:p.Gln1201=
NM_024577.3:c.3602A= , LRG_269t1:c.3602A= NP_078853.2:p.Gln1201=
NM_024577.4:c.3602A= MANE Select NP_078853.2:p.Gln1201=