Canonical Allele Identifier: CA1590312542

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027668A= , CM000667.2:g.149027668A=	GRCh38
NC_000005.9:g.148407231A= , CM000667.1:g.148407231A=	GRCh37
NC_000005.8:g.148387424A=	NCBI36
NG_007947.2:g.40507T= , LRG_269:g.40507T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1960T=
ENST00000515425.6:c.2064T= MANE Select	ENSP00000423660.1:p.Leu688=
ENST00000675793.1:c.*1348T=	ENSP00000502039.1:n.*1348T=
ENST00000676056.1:c.*1574T=	ENSP00000501827.1:n.*1574T=
ENST00000323829.9:c.*1452T=	ENSP00000313025.5:n.*1452T=
ENST00000504517.5:c.1594T=	ENSP00000421779.1:n.1594T=
ENST00000504690.5:c.2064T=	ENSP00000425627.1:p.Leu688=
ENST00000510779.1:c.1114T=
ENST00000511307.5:c.*1844T=	ENSP00000421420.1:n.*1844T=
ENST00000512049.5:c.2043T=	ENSP00000421860.1:p.Leu681=
ENST00000513604.5:c.*1452T=	ENSP00000423111.1:n.*1452T=
ENST00000515425.5:c.2064T=	ENSP00000423660.1:p.Leu688=
NM_024577.3:c.2064T= , LRG_269t1:c.2064T=	NP_078853.2:p.Leu688=
NM_024577.4:c.2064T= MANE Select	NP_078853.2:p.Leu688=