Canonical Allele Identifier: CA1590297793

Gene: SH3TC2

Linked Data

• dbSNP Id: rs1753475627

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148994639_148994640insCTGG , CM000667.2:g.148994639_148994640insCTGG	GRCh38
NC_000005.9:g.148374202_148374203insCTGG , CM000667.1:g.148374202_148374203insCTGG	GRCh37
NC_000005.8:g.148354395_148354396insCTGG	NCBI36
NG_007947.2:g.73538_73539insGCCA , LRG_269:g.73538_73539insGCCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000515425.6:c.*10074_*10075insGCCA MANE Select	ENSP00000423660.1:n.*10074_*10075insGCCA
ENST00000504690.5:c.*12+9089_*12+9090insGCCA	ENSP00000425627.1:n.*12+9089_*12+9090insGCCA
ENST00000510350.1:n.231+12244_231+12245insGCCA
NM_024577.3:c.*10074_*10075insGCCA , LRG_269t1:c.*10074_*10075insGCCA	NP_078853.2:n.*10074_*10075insGCCA
NM_024577.4:c.*10074_*10075insGCCA MANE Select	NP_078853.2:n.*10074_*10075insGCCA