Canonical Allele Identifier: CA1590312556

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027693T= , CM000667.2:g.149027693T=	GRCh38
NC_000005.9:g.148407256T= , CM000667.1:g.148407256T=	GRCh37
NC_000005.8:g.148387449T=	NCBI36
NG_007947.2:g.40482A= , LRG_269:g.40482A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1935A=
ENST00000515425.6:c.2039A= MANE Select	ENSP00000423660.1:p.Tyr680=
ENST00000675793.1:c.*1323A=	ENSP00000502039.1:n.*1323A=
ENST00000676056.1:c.*1549A=	ENSP00000501827.1:n.*1549A=
ENST00000323829.9:c.*1427A=	ENSP00000313025.5:n.*1427A=
ENST00000504517.5:c.1569A=	ENSP00000421779.1:n.1569A=
ENST00000504690.5:c.2039A=	ENSP00000425627.1:p.Tyr680=
ENST00000510779.1:c.1089A=
ENST00000511307.5:c.*1819A=	ENSP00000421420.1:n.*1819A=
ENST00000512049.5:c.2018A=	ENSP00000421860.1:p.Tyr673=
ENST00000513604.5:c.*1427A=	ENSP00000423111.1:n.*1427A=
ENST00000515425.5:c.2039A=	ENSP00000423660.1:p.Tyr680=
NM_024577.3:c.2039A= , LRG_269t1:c.2039A=	NP_078853.2:p.Tyr680=
NM_024577.4:c.2039A= MANE Select	NP_078853.2:p.Tyr680=