Canonical Allele Identifier: CA1590304222

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008868C= , CM000667.2:g.149008868C=	GRCh38
NC_000005.9:g.148388431C= , CM000667.1:g.148388431C=	GRCh37
NC_000005.8:g.148368624C=	NCBI36
NG_007947.2:g.59307G= , LRG_269:g.59307G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3357G=
ENST00000515425.6:c.3461G= MANE Select	ENSP00000423660.1:p.Arg1154=
ENST00000675793.1:c.*2745G=	ENSP00000502039.1:n.*2745G=
ENST00000323829.9:c.*2849G=	ENSP00000313025.5:n.*2849G=
ENST00000504517.5:c.2991G=	ENSP00000421779.1:n.2991G=
ENST00000504690.5:c.3461G=	ENSP00000425627.1:p.Arg1154=
ENST00000510779.1:c.2511G=
ENST00000512049.5:c.3440G=	ENSP00000421860.1:p.Arg1147=
ENST00000515229.5:n.123G=
ENST00000515425.5:c.3461G=	ENSP00000423660.1:p.Arg1154=
NM_024577.3:c.3461G= , LRG_269t1:c.3461G=	NP_078853.2:p.Arg1154=
NM_024577.4:c.3461G= MANE Select	NP_078853.2:p.Arg1154=