Canonical Allele Identifier: CA1590312535

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027647T= , CM000667.2:g.149027647T=	GRCh38
NC_000005.9:g.148407210T= , CM000667.1:g.148407210T=	GRCh37
NC_000005.8:g.148387403T=	NCBI36
NG_007947.2:g.40528A= , LRG_269:g.40528A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1981A=
ENST00000515425.6:c.2085A= MANE Select	ENSP00000423660.1:p.Gln695=
ENST00000675793.1:c.*1369A=	ENSP00000502039.1:n.*1369A=
ENST00000676056.1:c.*1595A=	ENSP00000501827.1:n.*1595A=
ENST00000323829.9:c.*1473A=	ENSP00000313025.5:n.*1473A=
ENST00000504517.5:c.1615A=	ENSP00000421779.1:n.1615A=
ENST00000504690.5:c.2085A=	ENSP00000425627.1:p.Gln695=
ENST00000510779.1:c.1135A=
ENST00000511307.5:c.*1865A=	ENSP00000421420.1:n.*1865A=
ENST00000512049.5:c.2064A=	ENSP00000421860.1:p.Gln688=
ENST00000513604.5:c.*1473A=	ENSP00000423111.1:n.*1473A=
ENST00000515425.5:c.2085A=	ENSP00000423660.1:p.Gln695=
NM_024577.3:c.2085A= , LRG_269t1:c.2085A=	NP_078853.2:p.Gln695=
NM_024577.4:c.2085A= MANE Select	NP_078853.2:p.Gln695=