Canonical Allele Identifier: CA1590312453

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027448T= , CM000667.2:g.149027448T=	GRCh38
NC_000005.9:g.148407011T= , CM000667.1:g.148407011T=	GRCh37
NC_000005.8:g.148387204T=	NCBI36
NG_007947.2:g.40727A= , LRG_269:g.40727A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.2180A=
ENST00000515425.6:c.2284A= MANE Select	ENSP00000423660.1:p.Ile762=
ENST00000675793.1:c.*1568A=	ENSP00000502039.1:n.*1568A=
ENST00000676056.1:c.*1794A=	ENSP00000501827.1:n.*1794A=
ENST00000323829.9:c.*1672A=	ENSP00000313025.5:n.*1672A=
ENST00000504517.5:c.1814A=	ENSP00000421779.1:n.1814A=
ENST00000504690.5:c.2284A=	ENSP00000425627.1:p.Ile762=
ENST00000510779.1:c.1334A=
ENST00000511307.5:c.*2064A=	ENSP00000421420.1:n.*2064A=
ENST00000512049.5:c.2263A=	ENSP00000421860.1:p.Ile755=
ENST00000513604.5:c.*1672A=	ENSP00000423111.1:n.*1672A=
ENST00000515425.5:c.2284A=	ENSP00000423660.1:p.Ile762=
NM_024577.3:c.2284A= , LRG_269t1:c.2284A=	NP_078853.2:p.Ile762=
NM_024577.4:c.2284A= MANE Select	NP_078853.2:p.Ile762=