Canonical Allele Identifier: CA1590303361
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149006955G= , CM000667.2:g.149006955G= GRCh38
NC_000005.9:g.148386518G= , CM000667.1:g.148386518G= GRCh37
NC_000005.8:g.148366711G= NCBI36
NG_007947.2:g.61220C= , LRG_269:g.61220C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502274.2:c.4454C=
ENST00000515425.6:c.3601C= MANE Select ENSP00000423660.1:p.Gln1201=
ENST00000675793.1:c.*4658C= ENSP00000502039.1:n.*4658C=
ENST00000323829.9:c.*2989C= ENSP00000313025.5:n.*2989C=
ENST00000502274.1:c.187C= ENSP00000421092.1:p.Gln63=
ENST00000504517.5:c.3123C= ENSP00000421779.1:n.3123C=
ENST00000504690.5:c.3601C= ENSP00000425627.1:p.Gln1201=
ENST00000510350.1:n.157C=
ENST00000510779.1:c.2651C=
ENST00000512049.5:c.3580C= ENSP00000421860.1:p.Gln1194=
ENST00000515229.5:n.263C=
ENST00000515425.5:c.3601C= ENSP00000423660.1:p.Gln1201=
NM_024577.3:c.3601C= , LRG_269t1:c.3601C= NP_078853.2:p.Gln1201=
NM_024577.4:c.3601C= MANE Select NP_078853.2:p.Gln1201=