Canonical Allele Identifier: CA1590312699

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027999A= , CM000667.2:g.149027999A=	GRCh38
NC_000005.9:g.148407562A= , CM000667.1:g.148407562A=	GRCh37
NC_000005.8:g.148387755A=	NCBI36
NG_007947.2:g.40176T= , LRG_269:g.40176T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1629T=
ENST00000515425.6:c.1733T= MANE Select	ENSP00000423660.1:p.Ile578=
ENST00000675793.1:c.*1017T=	ENSP00000502039.1:n.*1017T=
ENST00000676056.1:c.*1243T=	ENSP00000501827.1:n.*1243T=
ENST00000323829.9:c.*1121T=	ENSP00000313025.5:n.*1121T=
ENST00000504517.5:c.1263T=	ENSP00000421779.1:n.1263T=
ENST00000504690.5:c.1733T=	ENSP00000425627.1:p.Ile578=
ENST00000510779.1:c.783T=
ENST00000511307.5:c.*1513T=	ENSP00000421420.1:n.*1513T=
ENST00000512049.5:c.1712T=	ENSP00000421860.1:p.Ile571=
ENST00000513604.5:c.*1121T=	ENSP00000423111.1:n.*1121T=
ENST00000515425.5:c.1733T=	ENSP00000423660.1:p.Ile578=
NM_024577.3:c.1733T= , LRG_269t1:c.1733T=	NP_078853.2:p.Ile578=
NM_024577.4:c.1733T= MANE Select	NP_078853.2:p.Ile578=