Canonical Allele Identifier: CA1590317289

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149038295A= , CM000667.2:g.149038295A=	GRCh38
NC_000005.9:g.148417858A= , CM000667.1:g.148417858A=	GRCh37
NC_000005.8:g.148398051A=	NCBI36
NG_007947.2:g.29880T= , LRG_269:g.29880T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.891T=
ENST00000515425.6:c.1001T= MANE Select	ENSP00000423660.1:p.Met334=
ENST00000674655.1:c.263T=	ENSP00000502840.1:p.Ile88=
ENST00000674983.1:c.*259T=	ENSP00000502387.1:n.*259T=
ENST00000675793.1:c.1001T=	ENSP00000502039.1:p.Ile334=
ENST00000676056.1:c.*259T=	ENSP00000501827.1:n.*259T=
ENST00000323829.9:c.*259T=	ENSP00000313025.5:n.*259T=
ENST00000503071.1:n.468T=
ENST00000504517.5:c.401T=	ENSP00000421779.1:p.Met134=
ENST00000504690.5:c.1001T=	ENSP00000425627.1:p.Met334=
ENST00000511307.5:c.*781T=	ENSP00000421420.1:n.*781T=
ENST00000512049.5:c.980T=	ENSP00000421860.1:p.Met327=
ENST00000513604.5:c.*259T=	ENSP00000423111.1:n.*259T=
ENST00000515425.5:c.1001T=	ENSP00000423660.1:p.Met334=
NM_024577.3:c.1001T= , LRG_269t1:c.1001T=	NP_078853.2:p.Met334=
NM_024577.4:c.1001T= MANE Select	NP_078853.2:p.Met334=