Canonical Allele Identifier: CA1590312618

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027811G= , CM000667.2:g.149027811G=	GRCh38
NC_000005.9:g.148407374G= , CM000667.1:g.148407374G=	GRCh37
NC_000005.8:g.148387567G=	NCBI36
NG_007947.2:g.40364C= , LRG_269:g.40364C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1817C=
ENST00000515425.6:c.1921C= MANE Select	ENSP00000423660.1:p.Arg641=
ENST00000675793.1:c.*1205C=	ENSP00000502039.1:n.*1205C=
ENST00000676056.1:c.*1431C=	ENSP00000501827.1:n.*1431C=
ENST00000323829.9:c.*1309C=	ENSP00000313025.5:n.*1309C=
ENST00000504517.5:c.1451C=	ENSP00000421779.1:n.1451C=
ENST00000504690.5:c.1921C=	ENSP00000425627.1:p.Arg641=
ENST00000510779.1:c.971C=
ENST00000511307.5:c.*1701C=	ENSP00000421420.1:n.*1701C=
ENST00000512049.5:c.1900C=	ENSP00000421860.1:p.Arg634=
ENST00000513604.5:c.*1309C=	ENSP00000423111.1:n.*1309C=
ENST00000515425.5:c.1921C=	ENSP00000423660.1:p.Arg641=
NM_024577.3:c.1921C= , LRG_269t1:c.1921C=	NP_078853.2:p.Arg641=
NM_024577.4:c.1921C= MANE Select	NP_078853.2:p.Arg641=