Canonical Allele Identifier: CA1590303356

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149006948G= , CM000667.2:g.149006948G=	GRCh38
NC_000005.9:g.148386511G= , CM000667.1:g.148386511G=	GRCh37
NC_000005.8:g.148366704G=	NCBI36
NG_007947.2:g.61227C= , LRG_269:g.61227C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4461C=
ENST00000515425.6:c.3608C= MANE Select	ENSP00000423660.1:p.Pro1203=
ENST00000675793.1:c.*4665C=	ENSP00000502039.1:n.*4665C=
ENST00000323829.9:c.*2996C=	ENSP00000313025.5:n.*2996C=
ENST00000502274.1:c.194C=	ENSP00000421092.1:p.Pro65=
ENST00000504517.5:c.3130C=	ENSP00000421779.1:n.3130C=
ENST00000504690.5:c.3608C=	ENSP00000425627.1:p.Pro1203=
ENST00000510350.1:n.164C=
ENST00000510779.1:c.2658C=
ENST00000512049.5:c.3587C=	ENSP00000421860.1:p.Pro1196=
ENST00000515229.5:n.270C=
ENST00000515425.5:c.3608C=	ENSP00000423660.1:p.Pro1203=
NM_024577.3:c.3608C= , LRG_269t1:c.3608C=	NP_078853.2:p.Pro1203=
NM_024577.4:c.3608C= MANE Select	NP_078853.2:p.Pro1203=