Canonical Allele Identifier: CA1590312108

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026685G= , CM000667.2:g.149026685G=	GRCh38
NC_000005.9:g.148406248G= , CM000667.1:g.148406248G=	GRCh37
NC_000005.8:g.148386441G=	NCBI36
NG_007947.2:g.41490C= , LRG_269:g.41490C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2836C=
ENST00000515425.6:c.2940C= MANE Select	ENSP00000423660.1:p.Cys980=
ENST00000675793.1:c.*2224C=	ENSP00000502039.1:n.*2224C=
ENST00000676056.1:c.*2450C=	ENSP00000501827.1:n.*2450C=
ENST00000323829.9:c.*2328C=	ENSP00000313025.5:n.*2328C=
ENST00000504517.5:c.2470C=	ENSP00000421779.1:n.2470C=
ENST00000504690.5:c.2940C=	ENSP00000425627.1:p.Cys980=
ENST00000510779.1:c.1990C=
ENST00000511307.5:c.*2827C=	ENSP00000421420.1:n.*2827C=
ENST00000512049.5:c.2919C=	ENSP00000421860.1:p.Cys973=
ENST00000513604.5:c.*2435C=	ENSP00000423111.1:n.*2435C=
ENST00000515425.5:c.2940C=	ENSP00000423660.1:p.Cys980=
NM_024577.3:c.2940C= , LRG_269t1:c.2940C=	NP_078853.2:p.Cys980=
NM_024577.4:c.2940C= MANE Select	NP_078853.2:p.Cys980=