Canonical Allele Identifier: CA1590297713
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994577T= , CM000667.2:g.148994577T= GRCh38
NC_000005.9:g.148374140T= , CM000667.1:g.148374140T= GRCh37
NC_000005.8:g.148354333T= NCBI36
NG_007947.2:g.73598A= , LRG_269:g.73598A=

Transcript Alleles

HGVS Amino-acid change
ENST00000515425.6:c.*10134A= MANE Select ENSP00000423660.1:n.*10134A=
ENST00000504690.5:c.*12+9149A= ENSP00000425627.1:n.*12+9149A=
ENST00000510350.1:n.231+12304A=
NM_024577.3:c.*10134A= , LRG_269t1:c.*10134A= NP_078853.2:n.*10134A=
NM_024577.4:c.*10134A= MANE Select NP_078853.2:n.*10134A=