Canonical Allele Identifier: CA2839330006

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028127_149028129del , CM000667.2:g.149028127_149028129del	GRCh38
NC_000005.9:g.148407690_148407692del , CM000667.1:g.148407690_148407692del	GRCh37
NC_000005.8:g.148387883_148387885del	NCBI36
NG_007947.2:g.40046_40048del , LRG_269:g.40046_40048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1499_1501del
ENST00000515425.6:c.1603_1605del MANE Select	ENSP00000423660.1:p.Gly535del
ENST00000675793.1:c.*887_*889del	ENSP00000502039.1:n.*887_*889del
ENST00000676056.1:c.*1113_*1115del	ENSP00000501827.1:n.*1113_*1115del
ENST00000323829.9:c.*991_*993del	ENSP00000313025.5:n.*991_*993del
ENST00000504517.5:c.1133_1135del	ENSP00000421779.1:n.1133_1135del
ENST00000504690.5:c.1603_1605del	ENSP00000425627.1:p.Gly535del
ENST00000510779.1:c.653_655del
ENST00000511307.5:c.*1383_*1385del	ENSP00000421420.1:n.*1383_*1385del
ENST00000512049.5:c.1582_1584del	ENSP00000421860.1:p.Gly528del
ENST00000513604.5:c.*991_*993del	ENSP00000423111.1:n.*991_*993del
ENST00000515425.5:c.1603_1605del	ENSP00000423660.1:p.Gly535del
NM_024577.3:c.1603_1605del , LRG_269t1:c.1603_1605del	NP_078853.2:p.Gly535del
NM_024577.4:c.1603_1605del MANE Select	NP_078853.2:p.Gly535del