Canonical Allele Identifier: CA1590312539

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027659G= , CM000667.2:g.149027659G=	GRCh38
NC_000005.9:g.148407222G= , CM000667.1:g.148407222G=	GRCh37
NC_000005.8:g.148387415G=	NCBI36
NG_007947.2:g.40516C= , LRG_269:g.40516C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1969C=
ENST00000515425.6:c.2073C= MANE Select	ENSP00000423660.1:p.Ala691=
ENST00000675793.1:c.*1357C=	ENSP00000502039.1:n.*1357C=
ENST00000676056.1:c.*1583C=	ENSP00000501827.1:n.*1583C=
ENST00000323829.9:c.*1461C=	ENSP00000313025.5:n.*1461C=
ENST00000504517.5:c.1603C=	ENSP00000421779.1:n.1603C=
ENST00000504690.5:c.2073C=	ENSP00000425627.1:p.Ala691=
ENST00000510779.1:c.1123C=
ENST00000511307.5:c.*1853C=	ENSP00000421420.1:n.*1853C=
ENST00000512049.5:c.2052C=	ENSP00000421860.1:p.Ala684=
ENST00000513604.5:c.*1461C=	ENSP00000423111.1:n.*1461C=
ENST00000515425.5:c.2073C=	ENSP00000423660.1:p.Ala691=
NM_024577.3:c.2073C= , LRG_269t1:c.2073C=	NP_078853.2:p.Ala691=
NM_024577.4:c.2073C= MANE Select	NP_078853.2:p.Ala691=