Canonical Allele Identifier: CA1590297798
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994640_148994651delinsTTGGTTGGTTGG , CM000667.2:g.148994640_148994651delinsTTGGTTGGTTGG GRCh38
NC_000005.9:g.148374203_148374214delinsTTGGTTGGTTGG , CM000667.1:g.148374203_148374214delinsTTGGTTGGTTGG GRCh37
NC_000005.8:g.148354396_148354407delinsTTGGTTGGTTGG NCBI36
NG_007947.2:g.73524_73535delinsCCAACCAACCAA , LRG_269:g.73524_73535delinsCCAACCAACCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000515425.6:c.*10060_*10071delinsCCAACCAACCAA MANE Select ENSP00000423660.1:n.*10060_*10071delinsCCAACCAACCAA
ENST00000504690.5:c.*12+9075_*12+9086delinsCCAACCAACCAA ENSP00000425627.1:n.*12+9075_*12+9086delinsCCAACCAACCAA
ENST00000510350.1:n.231+12230_231+12241delinsCCAACCAACCAA
NM_024577.3:c.*10060_*10071delinsCCAACCAACCAA , LRG_269t1:c.*10060_*10071delinsCCAACCAACCAA NP_078853.2:n.*10060_*10071delinsCCAACCAACCAA
NM_024577.4:c.*10060_*10071delinsCCAACCAACCAA MANE Select NP_078853.2:n.*10060_*10071delinsCCAACCAACCAA