Canonical Allele Identifier: CA1590312203

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026878T= , CM000667.2:g.149026878T=	GRCh38
NC_000005.9:g.148406441T= , CM000667.1:g.148406441T=	GRCh37
NC_000005.8:g.148386634T=	NCBI36
NG_007947.2:g.41297A= , LRG_269:g.41297A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2750A=
ENST00000515425.6:c.2854A= MANE Select	ENSP00000423660.1:p.Arg952=
ENST00000675793.1:c.*2138A=	ENSP00000502039.1:n.*2138A=
ENST00000676056.1:c.*2364A=	ENSP00000501827.1:n.*2364A=
ENST00000323829.9:c.*2242A=	ENSP00000313025.5:n.*2242A=
ENST00000504517.5:c.2384A=	ENSP00000421779.1:n.2384A=
ENST00000504690.5:c.2854A=	ENSP00000425627.1:p.Arg952=
ENST00000510779.1:c.1904A=
ENST00000511307.5:c.*2634A=	ENSP00000421420.1:n.*2634A=
ENST00000512049.5:c.2833A=	ENSP00000421860.1:p.Arg945=
ENST00000513604.5:c.*2242A=	ENSP00000423111.1:n.*2242A=
ENST00000515425.5:c.2854A=	ENSP00000423660.1:p.Arg952=
NM_024577.3:c.2854A= , LRG_269t1:c.2854A=	NP_078853.2:p.Arg952=
NM_024577.4:c.2854A= MANE Select	NP_078853.2:p.Arg952=