Canonical Allele Identifier: CA3123355243

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027541C= , CM000667.2:g.149027541C=	GRCh38
NC_000005.9:g.148407104C= , CM000667.1:g.148407104C=	GRCh37
NC_000005.8:g.148387297C=	NCBI36
NG_007947.2:g.40634G= , LRG_269:g.40634G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2087G=
ENST00000515425.6:c.2191G= MANE Select	ENSP00000423660.1:p.Glu731=
ENST00000675793.1:c.*1475G=	ENSP00000502039.1:n.*1475G=
ENST00000676056.1:c.*1701G=	ENSP00000501827.1:n.*1701G=
ENST00000323829.9:c.*1579G=	ENSP00000313025.5:n.*1579G=
ENST00000504517.5:c.1721G=	ENSP00000421779.1:n.1721G=
ENST00000504690.5:c.2191G=	ENSP00000425627.1:p.Glu731=
ENST00000510779.1:c.1241G=
ENST00000511307.5:c.*1971G=	ENSP00000421420.1:n.*1971G=
ENST00000512049.5:c.2170G=	ENSP00000421860.1:p.Glu724=
ENST00000513604.5:c.*1579G=	ENSP00000423111.1:n.*1579G=
ENST00000515425.5:c.2191G=	ENSP00000423660.1:p.Glu731=
NM_024577.3:c.2191G= , LRG_269t1:c.2191G=	NP_078853.2:p.Glu731=
NM_024577.4:c.2191G= MANE Select	NP_078853.2:p.Glu731=