Canonical Allele Identifier: CA1590312538

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027654A= , CM000667.2:g.149027654A=	GRCh38
NC_000005.9:g.148407217A= , CM000667.1:g.148407217A=	GRCh37
NC_000005.8:g.148387410A=	NCBI36
NG_007947.2:g.40521T= , LRG_269:g.40521T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1974T=
ENST00000515425.6:c.2078T= MANE Select	ENSP00000423660.1:p.Val693=
ENST00000675793.1:c.*1362T=	ENSP00000502039.1:n.*1362T=
ENST00000676056.1:c.*1588T=	ENSP00000501827.1:n.*1588T=
ENST00000323829.9:c.*1466T=	ENSP00000313025.5:n.*1466T=
ENST00000504517.5:c.1608T=	ENSP00000421779.1:n.1608T=
ENST00000504690.5:c.2078T=	ENSP00000425627.1:p.Val693=
ENST00000510779.1:c.1128T=
ENST00000511307.5:c.*1858T=	ENSP00000421420.1:n.*1858T=
ENST00000512049.5:c.2057T=	ENSP00000421860.1:p.Val686=
ENST00000513604.5:c.*1466T=	ENSP00000423111.1:n.*1466T=
ENST00000515425.5:c.2078T=	ENSP00000423660.1:p.Val693=
NM_024577.3:c.2078T= , LRG_269t1:c.2078T=	NP_078853.2:p.Val693=
NM_024577.4:c.2078T= MANE Select	NP_078853.2:p.Val693=