Canonical Allele Identifier: CA1590312076

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026612C= , CM000667.2:g.149026612C=	GRCh38
NC_000005.9:g.148406175C= , CM000667.1:g.148406175C=	GRCh37
NC_000005.8:g.148386368C=	NCBI36
NG_007947.2:g.41563G= , LRG_269:g.41563G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2909G=
ENST00000515425.6:c.3013G= MANE Select	ENSP00000423660.1:p.Glu1005=
ENST00000675793.1:c.*2297G=	ENSP00000502039.1:n.*2297G=
ENST00000676056.1:c.*2523G=	ENSP00000501827.1:n.*2523G=
ENST00000323829.9:c.*2401G=	ENSP00000313025.5:n.*2401G=
ENST00000504517.5:c.2543G=	ENSP00000421779.1:n.2543G=
ENST00000504690.5:c.3013G=	ENSP00000425627.1:p.Glu1005=
ENST00000510779.1:c.2063G=
ENST00000511307.5:c.*2900G=	ENSP00000421420.1:n.*2900G=
ENST00000512049.5:c.2992G=	ENSP00000421860.1:p.Glu998=
ENST00000513604.5:c.*2508G=	ENSP00000423111.1:n.*2508G=
ENST00000515425.5:c.3013G=	ENSP00000423660.1:p.Glu1005=
NM_024577.3:c.3013G= , LRG_269t1:c.3013G=	NP_078853.2:p.Glu1005=
NM_024577.4:c.3013G= MANE Select	NP_078853.2:p.Glu1005=