Canonical Allele Identifier: CA1590312492

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027542A= , CM000667.2:g.149027542A=	GRCh38
NC_000005.9:g.148407105A= , CM000667.1:g.148407105A=	GRCh37
NC_000005.8:g.148387298A=	NCBI36
NG_007947.2:g.40633T= , LRG_269:g.40633T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.2086T=
ENST00000515425.6:c.2190T= MANE Select	ENSP00000423660.1:p.Gly730=
ENST00000675793.1:c.*1474T=	ENSP00000502039.1:n.*1474T=
ENST00000676056.1:c.*1700T=	ENSP00000501827.1:n.*1700T=
ENST00000323829.9:c.*1578T=	ENSP00000313025.5:n.*1578T=
ENST00000504517.5:c.1720T=	ENSP00000421779.1:n.1720T=
ENST00000504690.5:c.2190T=	ENSP00000425627.1:p.Gly730=
ENST00000510779.1:c.1240T=
ENST00000511307.5:c.*1970T=	ENSP00000421420.1:n.*1970T=
ENST00000512049.5:c.2169T=	ENSP00000421860.1:p.Gly723=
ENST00000513604.5:c.*1578T=	ENSP00000423111.1:n.*1578T=
ENST00000515425.5:c.2190T=	ENSP00000423660.1:p.Gly730=
NM_024577.3:c.2190T= , LRG_269t1:c.2190T=	NP_078853.2:p.Gly730=
NM_024577.4:c.2190T= MANE Select	NP_078853.2:p.Gly730=