Canonical Allele Identifier: CA1139659132

Gene: SH3TC2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027242_149027245del , CM000667.2:g.149027242_149027245del	GRCh38
NC_000005.9:g.148406805_148406808del , CM000667.1:g.148406805_148406808del	GRCh37
NC_000005.8:g.148386998_148387001del	NCBI36
NG_007947.2:g.40932_40935del , LRG_269:g.40932_40935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2385_2388del
ENST00000515425.6:c.2489_2492del MANE Select	ENSP00000423660.1:p.Glu830ValfsTer22
ENST00000675793.1:c.*1773_*1776del	ENSP00000502039.1:n.*1773_*1776del
ENST00000676056.1:c.*1999_*2002del	ENSP00000501827.1:n.*1999_*2002del
ENST00000323829.9:c.*1877_*1880del	ENSP00000313025.5:n.*1877_*1880del
ENST00000504517.5:c.2019_2022del	ENSP00000421779.1:n.2019_2022del
ENST00000504690.5:c.2489_2492del	ENSP00000425627.1:p.Glu830ValfsTer22
ENST00000510779.1:c.1539_1542del
ENST00000511307.5:c.*2269_*2272del	ENSP00000421420.1:n.*2269_*2272del
ENST00000512049.5:c.2468_2471del	ENSP00000421860.1:p.Glu823ValfsTer22
ENST00000513604.5:c.*1877_*1880del	ENSP00000423111.1:n.*1877_*1880del
ENST00000515425.5:c.2489_2492del	ENSP00000423660.1:p.Glu830ValfsTer22
NM_024577.3:c.2489_2492del , LRG_269t1:c.2489_2492del	NP_078853.2:p.Glu830ValfsTer22
NM_024577.4:c.2489_2492del MANE Select	NP_078853.2:p.Glu830ValfsTer22