Canonical Allele Identifier: CA1590312072

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026606G= , CM000667.2:g.149026606G=	GRCh38
NC_000005.9:g.148406169G= , CM000667.1:g.148406169G=	GRCh37
NC_000005.8:g.148386362G=	NCBI36
NG_007947.2:g.41569C= , LRG_269:g.41569C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2915C=
ENST00000515425.6:c.3019C= MANE Select	ENSP00000423660.1:p.Leu1007=
ENST00000675793.1:c.*2303C=	ENSP00000502039.1:n.*2303C=
ENST00000676056.1:c.*2529C=	ENSP00000501827.1:n.*2529C=
ENST00000323829.9:c.*2407C=	ENSP00000313025.5:n.*2407C=
ENST00000504517.5:c.2549C=	ENSP00000421779.1:n.2549C=
ENST00000504690.5:c.3019C=	ENSP00000425627.1:p.Leu1007=
ENST00000510779.1:c.2069C=
ENST00000511307.5:c.*2906C=	ENSP00000421420.1:n.*2906C=
ENST00000512049.5:c.2998C=	ENSP00000421860.1:p.Leu1000=
ENST00000513604.5:c.*2514C=	ENSP00000423111.1:n.*2514C=
ENST00000515425.5:c.3019C=	ENSP00000423660.1:p.Leu1007=
NM_024577.3:c.3019C= , LRG_269t1:c.3019C=	NP_078853.2:p.Leu1007=
NM_024577.4:c.3019C= MANE Select	NP_078853.2:p.Leu1007=