Canonical Allele Identifier: CA1590312210

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026903A= , CM000667.2:g.149026903A=	GRCh38
NC_000005.9:g.148406466A= , CM000667.1:g.148406466A=	GRCh37
NC_000005.8:g.148386659A=	NCBI36
NG_007947.2:g.41272T= , LRG_269:g.41272T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2725T=
ENST00000515425.6:c.2829T= MANE Select	ENSP00000423660.1:p.Tyr943=
ENST00000675793.1:c.*2113T=	ENSP00000502039.1:n.*2113T=
ENST00000676056.1:c.*2339T=	ENSP00000501827.1:n.*2339T=
ENST00000323829.9:c.*2217T=	ENSP00000313025.5:n.*2217T=
ENST00000504517.5:c.2359T=	ENSP00000421779.1:n.2359T=
ENST00000504690.5:c.2829T=	ENSP00000425627.1:p.Tyr943=
ENST00000510779.1:c.1879T=
ENST00000511307.5:c.*2609T=	ENSP00000421420.1:n.*2609T=
ENST00000512049.5:c.2808T=	ENSP00000421860.1:p.Tyr936=
ENST00000513604.5:c.*2217T=	ENSP00000423111.1:n.*2217T=
ENST00000515425.5:c.2829T=	ENSP00000423660.1:p.Tyr943=
NM_024577.3:c.2829T= , LRG_269t1:c.2829T=	NP_078853.2:p.Tyr943=
NM_024577.4:c.2829T= MANE Select	NP_078853.2:p.Tyr943=