Canonical Allele Identifier: CA1590304253

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008955T= , CM000667.2:g.149008955T=	GRCh38
NC_000005.9:g.148388518T= , CM000667.1:g.148388518T=	GRCh37
NC_000005.8:g.148368711T=	NCBI36
NG_007947.2:g.59220A= , LRG_269:g.59220A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3270A=
ENST00000515425.6:c.3374A= MANE Select	ENSP00000423660.1:p.Glu1125=
ENST00000675793.1:c.*2658A=	ENSP00000502039.1:n.*2658A=
ENST00000323829.9:c.*2762A=	ENSP00000313025.5:n.*2762A=
ENST00000504517.5:c.2904A=	ENSP00000421779.1:n.2904A=
ENST00000504690.5:c.3374A=	ENSP00000425627.1:p.Glu1125=
ENST00000510779.1:c.2424A=
ENST00000512049.5:c.3353A=	ENSP00000421860.1:p.Glu1118=
ENST00000515229.5:n.36A=
ENST00000515425.5:c.3374A=	ENSP00000423660.1:p.Glu1125=
NM_024577.3:c.3374A= , LRG_269t1:c.3374A=	NP_078853.2:p.Glu1125=
NM_024577.4:c.3374A= MANE Select	NP_078853.2:p.Glu1125=