Canonical Allele Identifier: CA1590312585

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027743A= , CM000667.2:g.149027743A=	GRCh38
NC_000005.9:g.148407306A= , CM000667.1:g.148407306A=	GRCh37
NC_000005.8:g.148387499A=	NCBI36
NG_007947.2:g.40432T= , LRG_269:g.40432T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1885T=
ENST00000515425.6:c.1989T= MANE Select	ENSP00000423660.1:p.Ser663=
ENST00000675793.1:c.*1273T=	ENSP00000502039.1:n.*1273T=
ENST00000676056.1:c.*1499T=	ENSP00000501827.1:n.*1499T=
ENST00000323829.9:c.*1377T=	ENSP00000313025.5:n.*1377T=
ENST00000504517.5:c.1519T=	ENSP00000421779.1:n.1519T=
ENST00000504690.5:c.1989T=	ENSP00000425627.1:p.Ser663=
ENST00000510779.1:c.1039T=
ENST00000511307.5:c.*1769T=	ENSP00000421420.1:n.*1769T=
ENST00000512049.5:c.1968T=	ENSP00000421860.1:p.Ser656=
ENST00000513604.5:c.*1377T=	ENSP00000423111.1:n.*1377T=
ENST00000515425.5:c.1989T=	ENSP00000423660.1:p.Ser663=
NM_024577.3:c.1989T= , LRG_269t1:c.1989T=	NP_078853.2:p.Ser663=
NM_024577.4:c.1989T= MANE Select	NP_078853.2:p.Ser663=