Canonical Allele Identifier: CA1590303400

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149007045G= , CM000667.2:g.149007045G=	GRCh38
NC_000005.9:g.148386608G= , CM000667.1:g.148386608G=	GRCh37
NC_000005.8:g.148366801G=	NCBI36
NG_007947.2:g.61130C= , LRG_269:g.61130C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4364C=
ENST00000515425.6:c.3511C= MANE Select	ENSP00000423660.1:p.Arg1171=
ENST00000675793.1:c.*4568C=	ENSP00000502039.1:n.*4568C=
ENST00000323829.9:c.*2899C=	ENSP00000313025.5:n.*2899C=
ENST00000502274.1:c.97C=	ENSP00000421092.1:p.Arg33=
ENST00000504517.5:c.3033C=	ENSP00000421779.1:n.3033C=
ENST00000504690.5:c.3511C=	ENSP00000425627.1:p.Arg1171=
ENST00000510350.1:n.67C=
ENST00000510779.1:c.2561C=
ENST00000512049.5:c.3490C=	ENSP00000421860.1:p.Arg1164=
ENST00000515229.5:n.173C=
ENST00000515425.5:c.3511C=	ENSP00000423660.1:p.Arg1171=
NM_024577.3:c.3511C= , LRG_269t1:c.3511C=	NP_078853.2:p.Arg1171=
NM_024577.4:c.3511C= MANE Select	NP_078853.2:p.Arg1171=