Canonical Allele Identifier: CA1590312075

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026611T= , CM000667.2:g.149026611T=	GRCh38
NC_000005.9:g.148406174T= , CM000667.1:g.148406174T=	GRCh37
NC_000005.8:g.148386367T=	NCBI36
NG_007947.2:g.41564A= , LRG_269:g.41564A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2910A=
ENST00000515425.6:c.3014A= MANE Select	ENSP00000423660.1:p.Glu1005=
ENST00000675793.1:c.*2298A=	ENSP00000502039.1:n.*2298A=
ENST00000676056.1:c.*2524A=	ENSP00000501827.1:n.*2524A=
ENST00000323829.9:c.*2402A=	ENSP00000313025.5:n.*2402A=
ENST00000504517.5:c.2544A=	ENSP00000421779.1:n.2544A=
ENST00000504690.5:c.3014A=	ENSP00000425627.1:p.Glu1005=
ENST00000510779.1:c.2064A=
ENST00000511307.5:c.*2901A=	ENSP00000421420.1:n.*2901A=
ENST00000512049.5:c.2993A=	ENSP00000421860.1:p.Glu998=
ENST00000513604.5:c.*2509A=	ENSP00000423111.1:n.*2509A=
ENST00000515425.5:c.3014A=	ENSP00000423660.1:p.Glu1005=
NM_024577.3:c.3014A= , LRG_269t1:c.3014A=	NP_078853.2:p.Glu1005=
NM_024577.4:c.3014A= MANE Select	NP_078853.2:p.Glu1005=