Canonical Allele Identifier: CA1590297770
Gene: SH3TC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994620T= , CM000667.2:g.148994620T= GRCh38
NC_000005.9:g.148374183T= , CM000667.1:g.148374183T= GRCh37
NC_000005.8:g.148354376T= NCBI36
NG_007947.2:g.73555A= , LRG_269:g.73555A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10091A= MANE Select ENSP00000423660.1:n.*10091A=
ENST00000504690.5:c.*12+9106A= ENSP00000425627.1:n.*12+9106A=
ENST00000510350.1:n.231+12261A=
NM_024577.3:c.*10091A= , LRG_269t1:c.*10091A= NP_078853.2:n.*10091A=
NM_024577.4:c.*10091A= MANE Select NP_078853.2:n.*10091A=
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