Canonical Allele Identifier: CA1590312719

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028054C= , CM000667.2:g.149028054C=	GRCh38
NC_000005.9:g.148407617C= , CM000667.1:g.148407617C=	GRCh37
NC_000005.8:g.148387810C=	NCBI36
NG_007947.2:g.40121G= , LRG_269:g.40121G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1574G=
ENST00000515425.6:c.1678G= MANE Select	ENSP00000423660.1:p.Gly560=
ENST00000675793.1:c.*962G=	ENSP00000502039.1:n.*962G=
ENST00000676056.1:c.*1188G=	ENSP00000501827.1:n.*1188G=
ENST00000323829.9:c.*1066G=	ENSP00000313025.5:n.*1066G=
ENST00000504517.5:c.1208G=	ENSP00000421779.1:n.1208G=
ENST00000504690.5:c.1678G=	ENSP00000425627.1:p.Gly560=
ENST00000510779.1:c.728G=
ENST00000511307.5:c.*1458G=	ENSP00000421420.1:n.*1458G=
ENST00000512049.5:c.1657G=	ENSP00000421860.1:p.Gly553=
ENST00000513604.5:c.*1066G=	ENSP00000423111.1:n.*1066G=
ENST00000515425.5:c.1678G=	ENSP00000423660.1:p.Gly560=
NM_024577.3:c.1678G= , LRG_269t1:c.1678G=	NP_078853.2:p.Gly560=
NM_024577.4:c.1678G= MANE Select	NP_078853.2:p.Gly560=