Canonical Allele Identifier: CA1590312572

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027724C= , CM000667.2:g.149027724C=	GRCh38
NC_000005.9:g.148407287C= , CM000667.1:g.148407287C=	GRCh37
NC_000005.8:g.148387480C=	NCBI36
NG_007947.2:g.40451G= , LRG_269:g.40451G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1904G=
ENST00000515425.6:c.2008G= MANE Select	ENSP00000423660.1:p.Glu670=
ENST00000675793.1:c.*1292G=	ENSP00000502039.1:n.*1292G=
ENST00000676056.1:c.*1518G=	ENSP00000501827.1:n.*1518G=
ENST00000323829.9:c.*1396G=	ENSP00000313025.5:n.*1396G=
ENST00000504517.5:c.1538G=	ENSP00000421779.1:n.1538G=
ENST00000504690.5:c.2008G=	ENSP00000425627.1:p.Glu670=
ENST00000510779.1:c.1058G=
ENST00000511307.5:c.*1788G=	ENSP00000421420.1:n.*1788G=
ENST00000512049.5:c.1987G=	ENSP00000421860.1:p.Glu663=
ENST00000513604.5:c.*1396G=	ENSP00000423111.1:n.*1396G=
ENST00000515425.5:c.2008G=	ENSP00000423660.1:p.Glu670=
NM_024577.3:c.2008G= , LRG_269t1:c.2008G=	NP_078853.2:p.Glu670=
NM_024577.4:c.2008G= MANE Select	NP_078853.2:p.Glu670=