Canonical Allele Identifier: CA1590312464

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027474C= , CM000667.2:g.149027474C=	GRCh38
NC_000005.9:g.148407037C= , CM000667.1:g.148407037C=	GRCh37
NC_000005.8:g.148387230C=	NCBI36
NG_007947.2:g.40701G= , LRG_269:g.40701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2154G=
ENST00000515425.6:c.2258G= MANE Select	ENSP00000423660.1:p.Arg753=
ENST00000675793.1:c.*1542G=	ENSP00000502039.1:n.*1542G=
ENST00000676056.1:c.*1768G=	ENSP00000501827.1:n.*1768G=
ENST00000323829.9:c.*1646G=	ENSP00000313025.5:n.*1646G=
ENST00000504517.5:c.1788G=	ENSP00000421779.1:n.1788G=
ENST00000504690.5:c.2258G=	ENSP00000425627.1:p.Arg753=
ENST00000510779.1:c.1308G=
ENST00000511307.5:c.*2038G=	ENSP00000421420.1:n.*2038G=
ENST00000512049.5:c.2237G=	ENSP00000421860.1:p.Arg746=
ENST00000513604.5:c.*1646G=	ENSP00000423111.1:n.*1646G=
ENST00000515425.5:c.2258G=	ENSP00000423660.1:p.Arg753=
NM_024577.3:c.2258G= , LRG_269t1:c.2258G=	NP_078853.2:p.Arg753=
NM_024577.4:c.2258G= MANE Select	NP_078853.2:p.Arg753=