Canonical Allele Identifier: CA1590312201

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026876C= , CM000667.2:g.149026876C=	GRCh38
NC_000005.9:g.148406439C= , CM000667.1:g.148406439C=	GRCh37
NC_000005.8:g.148386632C=	NCBI36
NG_007947.2:g.41299G= , LRG_269:g.41299G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2752G=
ENST00000515425.6:c.2856G= MANE Select	ENSP00000423660.1:p.Arg952=
ENST00000675793.1:c.*2140G=	ENSP00000502039.1:n.*2140G=
ENST00000676056.1:c.*2366G=	ENSP00000501827.1:n.*2366G=
ENST00000323829.9:c.*2244G=	ENSP00000313025.5:n.*2244G=
ENST00000504517.5:c.2386G=	ENSP00000421779.1:n.2386G=
ENST00000504690.5:c.2856G=	ENSP00000425627.1:p.Arg952=
ENST00000510779.1:c.1906G=
ENST00000511307.5:c.*2636G=	ENSP00000421420.1:n.*2636G=
ENST00000512049.5:c.2835G=	ENSP00000421860.1:p.Arg945=
ENST00000513604.5:c.*2244G=	ENSP00000423111.1:n.*2244G=
ENST00000515425.5:c.2856G=	ENSP00000423660.1:p.Arg952=
NM_024577.3:c.2856G= , LRG_269t1:c.2856G=	NP_078853.2:p.Arg952=
NM_024577.4:c.2856G= MANE Select	NP_078853.2:p.Arg952=