Canonical Allele Identifier: CA1590312498

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027549C= , CM000667.2:g.149027549C=	GRCh38
NC_000005.9:g.148407112C= , CM000667.1:g.148407112C=	GRCh37
NC_000005.8:g.148387305C=	NCBI36
NG_007947.2:g.40626G= , LRG_269:g.40626G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.2079G=
ENST00000515425.6:c.2183G= MANE Select	ENSP00000423660.1:p.Gly728=
ENST00000675793.1:c.*1467G=	ENSP00000502039.1:n.*1467G=
ENST00000676056.1:c.*1693G=	ENSP00000501827.1:n.*1693G=
ENST00000323829.9:c.*1571G=	ENSP00000313025.5:n.*1571G=
ENST00000504517.5:c.1713G=	ENSP00000421779.1:n.1713G=
ENST00000504690.5:c.2183G=	ENSP00000425627.1:p.Gly728=
ENST00000510779.1:c.1233G=
ENST00000511307.5:c.*1963G=	ENSP00000421420.1:n.*1963G=
ENST00000512049.5:c.2162G=	ENSP00000421860.1:p.Gly721=
ENST00000513604.5:c.*1571G=	ENSP00000423111.1:n.*1571G=
ENST00000515425.5:c.2183G=	ENSP00000423660.1:p.Gly728=
NM_024577.3:c.2183G= , LRG_269t1:c.2183G=	NP_078853.2:p.Gly728=
NM_024577.4:c.2183G= MANE Select	NP_078853.2:p.Gly728=