Canonical Allele Identifier: CA1590312107

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026684T= , CM000667.2:g.149026684T=	GRCh38
NC_000005.9:g.148406247T= , CM000667.1:g.148406247T=	GRCh37
NC_000005.8:g.148386440T=	NCBI36
NG_007947.2:g.41491A= , LRG_269:g.41491A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2837A=
ENST00000515425.6:c.2941A= MANE Select	ENSP00000423660.1:p.Ile981=
ENST00000675793.1:c.*2225A=	ENSP00000502039.1:n.*2225A=
ENST00000676056.1:c.*2451A=	ENSP00000501827.1:n.*2451A=
ENST00000323829.9:c.*2329A=	ENSP00000313025.5:n.*2329A=
ENST00000504517.5:c.2471A=	ENSP00000421779.1:n.2471A=
ENST00000504690.5:c.2941A=	ENSP00000425627.1:p.Ile981=
ENST00000510779.1:c.1991A=
ENST00000511307.5:c.*2828A=	ENSP00000421420.1:n.*2828A=
ENST00000512049.5:c.2920A=	ENSP00000421860.1:p.Ile974=
ENST00000513604.5:c.*2436A=	ENSP00000423111.1:n.*2436A=
ENST00000515425.5:c.2941A=	ENSP00000423660.1:p.Ile981=
NM_024577.3:c.2941A= , LRG_269t1:c.2941A=	NP_078853.2:p.Ile981=
NM_024577.4:c.2941A= MANE Select	NP_078853.2:p.Ile981=