Canonical Allele Identifier: CA1590303358

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149006952T= , CM000667.2:g.149006952T=	GRCh38
NC_000005.9:g.148386515T= , CM000667.1:g.148386515T=	GRCh37
NC_000005.8:g.148366708T=	NCBI36
NG_007947.2:g.61223A= , LRG_269:g.61223A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4457A=
ENST00000515425.6:c.3604A= MANE Select	ENSP00000423660.1:p.Ser1202=
ENST00000675793.1:c.*4661A=	ENSP00000502039.1:n.*4661A=
ENST00000323829.9:c.*2992A=	ENSP00000313025.5:n.*2992A=
ENST00000502274.1:c.190A=	ENSP00000421092.1:p.Ser64=
ENST00000504517.5:c.3126A=	ENSP00000421779.1:n.3126A=
ENST00000504690.5:c.3604A=	ENSP00000425627.1:p.Ser1202=
ENST00000510350.1:n.160A=
ENST00000510779.1:c.2654A=
ENST00000512049.5:c.3583A=	ENSP00000421860.1:p.Ser1195=
ENST00000515229.5:n.266A=
ENST00000515425.5:c.3604A=	ENSP00000423660.1:p.Ser1202=
NM_024577.3:c.3604A= , LRG_269t1:c.3604A=	NP_078853.2:p.Ser1202=
NM_024577.4:c.3604A= MANE Select	NP_078853.2:p.Ser1202=