Canonical Allele Identifier: CA1590297807

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148994649_148994650delinsTG , CM000667.2:g.148994649_148994650delinsTG	GRCh38
NC_000005.9:g.148374212_148374213delinsTG , CM000667.1:g.148374212_148374213delinsTG	GRCh37
NC_000005.8:g.148354405_148354406delinsTG	NCBI36
NG_007947.2:g.73525_73526delinsCA , LRG_269:g.73525_73526delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000515425.6:c.*10061_*10062delinsCA MANE Select	ENSP00000423660.1:n.*10061_*10062delinsCA
ENST00000504690.5:c.*12+9076_*12+9077delinsCA	ENSP00000425627.1:n.*12+9076_*12+9077delinsCA
ENST00000510350.1:n.231+12231_231+12232delinsCA
NM_024577.3:c.*10061_*10062delinsCA , LRG_269t1:c.*10061_*10062delinsCA	NP_078853.2:n.*10061_*10062delinsCA
NM_024577.4:c.*10061_*10062delinsCA MANE Select	NP_078853.2:n.*10061_*10062delinsCA