Canonical Allele Identifier: CA1590312955

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028555C= , CM000667.2:g.149028555C=	GRCh38
NC_000005.9:g.148408118C= , CM000667.1:g.148408118C=	GRCh37
NC_000005.8:g.148388311C=	NCBI36
NG_007947.2:g.39620G= , LRG_269:g.39620G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024577.4:c.1178-1G= MANE Select	NP_078853.2:n.1178-1G=
ENST00000515425.6:c.1178-1G= MANE Select	ENSP00000423660.1:n.1178-1G=
NM_024577.3:c.1178-1G= , LRG_269t1:c.1178-1G=	NP_078853.2:n.1178-1G=
ENST00000323829.9:c.*566-1G=	ENSP00000313025.5:n.*566-1G=
ENST00000502274.2:c.1198-1G=
ENST00000504517.5:c.708-1G=	ENSP00000421779.1:n.708-1G=
ENST00000504690.5:c.1178-1G=	ENSP00000425627.1:n.1178-1G=
ENST00000510779.1:c.227G=
ENST00000511307.5:c.*958-1G=	ENSP00000421420.1:n.*958-1G=
ENST00000512049.5:c.1157-1G=	ENSP00000421860.1:n.1157-1G=
ENST00000513340.1:n.552-1G=
ENST00000513604.5:c.*566-1G=	ENSP00000423111.1:n.*566-1G=
ENST00000515425.5:c.1178-1G=	ENSP00000423660.1:n.1178-1G=
ENST00000675793.1:c.*462-1G=	ENSP00000502039.1:n.*462-1G=
ENST00000676056.1:c.*687G=	ENSP00000501827.1:n.*687G=