Canonical Allele Identifier: CA1590312078

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026618G= , CM000667.2:g.149026618G=	GRCh38
NC_000005.9:g.148406181G= , CM000667.1:g.148406181G=	GRCh37
NC_000005.8:g.148386374G=	NCBI36
NG_007947.2:g.41557C= , LRG_269:g.41557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2903C=
ENST00000515425.6:c.3007C= MANE Select	ENSP00000423660.1:p.Leu1003=
ENST00000675793.1:c.*2291C=	ENSP00000502039.1:n.*2291C=
ENST00000676056.1:c.*2517C=	ENSP00000501827.1:n.*2517C=
ENST00000323829.9:c.*2395C=	ENSP00000313025.5:n.*2395C=
ENST00000504517.5:c.2537C=	ENSP00000421779.1:n.2537C=
ENST00000504690.5:c.3007C=	ENSP00000425627.1:p.Leu1003=
ENST00000510779.1:c.2057C=
ENST00000511307.5:c.*2894C=	ENSP00000421420.1:n.*2894C=
ENST00000512049.5:c.2986C=	ENSP00000421860.1:p.Leu996=
ENST00000513604.5:c.*2502C=	ENSP00000423111.1:n.*2502C=
ENST00000515425.5:c.3007C=	ENSP00000423660.1:p.Leu1003=
NM_024577.3:c.3007C= , LRG_269t1:c.3007C=	NP_078853.2:p.Leu1003=
NM_024577.4:c.3007C= MANE Select	NP_078853.2:p.Leu1003=