Canonical Allele Identifier: CA1590312067

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026591G= , CM000667.2:g.149026591G=	GRCh38
NC_000005.9:g.148406154G= , CM000667.1:g.148406154G=	GRCh37
NC_000005.8:g.148386347G=	NCBI36
NG_007947.2:g.41584C= , LRG_269:g.41584C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2930C=
ENST00000515425.6:c.3034C= MANE Select	ENSP00000423660.1:p.Arg1012=
ENST00000675793.1:c.*2318C=	ENSP00000502039.1:n.*2318C=
ENST00000676056.1:c.*2544C=	ENSP00000501827.1:n.*2544C=
ENST00000323829.9:c.*2422C=	ENSP00000313025.5:n.*2422C=
ENST00000504517.5:c.2564C=	ENSP00000421779.1:n.2564C=
ENST00000504690.5:c.3034C=	ENSP00000425627.1:p.Arg1012=
ENST00000510779.1:c.2084C=
ENST00000511307.5:c.*2921C=	ENSP00000421420.1:n.*2921C=
ENST00000512049.5:c.3013C=	ENSP00000421860.1:p.Arg1005=
ENST00000513604.5:c.*2529C=	ENSP00000423111.1:n.*2529C=
ENST00000515425.5:c.3034C=	ENSP00000423660.1:p.Arg1012=
NM_024577.3:c.3034C= , LRG_269t1:c.3034C=	NP_078853.2:p.Arg1012=
NM_024577.4:c.3034C= MANE Select	NP_078853.2:p.Arg1012=