Canonical Allele Identifier: CA1590312615

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027806C= , CM000667.2:g.149027806C=	GRCh38
NC_000005.9:g.148407369C= , CM000667.1:g.148407369C=	GRCh37
NC_000005.8:g.148387562C=	NCBI36
NG_007947.2:g.40369G= , LRG_269:g.40369G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1822G=
ENST00000515425.6:c.1926G= MANE Select	ENSP00000423660.1:p.Leu642=
ENST00000675793.1:c.*1210G=	ENSP00000502039.1:n.*1210G=
ENST00000676056.1:c.*1436G=	ENSP00000501827.1:n.*1436G=
ENST00000323829.9:c.*1314G=	ENSP00000313025.5:n.*1314G=
ENST00000504517.5:c.1456G=	ENSP00000421779.1:n.1456G=
ENST00000504690.5:c.1926G=	ENSP00000425627.1:p.Leu642=
ENST00000510779.1:c.976G=
ENST00000511307.5:c.*1706G=	ENSP00000421420.1:n.*1706G=
ENST00000512049.5:c.1905G=	ENSP00000421860.1:p.Leu635=
ENST00000513604.5:c.*1314G=	ENSP00000423111.1:n.*1314G=
ENST00000515425.5:c.1926G=	ENSP00000423660.1:p.Leu642=
NM_024577.3:c.1926G= , LRG_269t1:c.1926G=	NP_078853.2:p.Leu642=
NM_024577.4:c.1926G= MANE Select	NP_078853.2:p.Leu642=