Canonical Allele Identifier: CA1590312679

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027945C= , CM000667.2:g.149027945C=	GRCh38
NC_000005.9:g.148407508C= , CM000667.1:g.148407508C=	GRCh37
NC_000005.8:g.148387701C=	NCBI36
NG_007947.2:g.40230G= , LRG_269:g.40230G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1683G=
ENST00000515425.6:c.1787G= MANE Select	ENSP00000423660.1:p.Gly596=
ENST00000675793.1:c.*1071G=	ENSP00000502039.1:n.*1071G=
ENST00000676056.1:c.*1297G=	ENSP00000501827.1:n.*1297G=
ENST00000323829.9:c.*1175G=	ENSP00000313025.5:n.*1175G=
ENST00000504517.5:c.1317G=	ENSP00000421779.1:n.1317G=
ENST00000504690.5:c.1787G=	ENSP00000425627.1:p.Gly596=
ENST00000510779.1:c.837G=
ENST00000511307.5:c.*1567G=	ENSP00000421420.1:n.*1567G=
ENST00000512049.5:c.1766G=	ENSP00000421860.1:p.Gly589=
ENST00000513604.5:c.*1175G=	ENSP00000423111.1:n.*1175G=
ENST00000515425.5:c.1787G=	ENSP00000423660.1:p.Gly596=
NM_024577.3:c.1787G= , LRG_269t1:c.1787G=	NP_078853.2:p.Gly596=
NM_024577.4:c.1787G= MANE Select	NP_078853.2:p.Gly596=