Canonical Allele Identifier: CA1590304250

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008946A= , CM000667.2:g.149008946A=	GRCh38
NC_000005.9:g.148388509A= , CM000667.1:g.148388509A=	GRCh37
NC_000005.8:g.148368702A=	NCBI36
NG_007947.2:g.59229T= , LRG_269:g.59229T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3279T=
ENST00000515425.6:c.3383T= MANE Select	ENSP00000423660.1:p.Ile1128=
ENST00000675793.1:c.*2667T=	ENSP00000502039.1:n.*2667T=
ENST00000323829.9:c.*2771T=	ENSP00000313025.5:n.*2771T=
ENST00000504517.5:c.2913T=	ENSP00000421779.1:n.2913T=
ENST00000504690.5:c.3383T=	ENSP00000425627.1:p.Ile1128=
ENST00000510779.1:c.2433T=
ENST00000512049.5:c.3362T=	ENSP00000421860.1:p.Ile1121=
ENST00000515229.5:n.45T=
ENST00000515425.5:c.3383T=	ENSP00000423660.1:p.Ile1128=
NM_024577.3:c.3383T= , LRG_269t1:c.3383T=	NP_078853.2:p.Ile1128=
NM_024577.4:c.3383T= MANE Select	NP_078853.2:p.Ile1128=