Canonical Allele Identifier: CA1590303354

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149006945T= , CM000667.2:g.149006945T=	GRCh38
NC_000005.9:g.148386508T= , CM000667.1:g.148386508T=	GRCh37
NC_000005.8:g.148366701T=	NCBI36
NG_007947.2:g.61230A= , LRG_269:g.61230A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4464A=
ENST00000515425.6:c.3611A= MANE Select	ENSP00000423660.1:p.Lys1204=
ENST00000675793.1:c.*4668A=	ENSP00000502039.1:n.*4668A=
ENST00000323829.9:c.*2999A=	ENSP00000313025.5:n.*2999A=
ENST00000502274.1:c.197A=	ENSP00000421092.1:p.Lys66=
ENST00000504517.5:c.3133A=	ENSP00000421779.1:n.3133A=
ENST00000504690.5:c.3611A=	ENSP00000425627.1:p.Lys1204=
ENST00000510350.1:n.167A=
ENST00000510779.1:c.2661A=
ENST00000512049.5:c.3590A=	ENSP00000421860.1:p.Lys1197=
ENST00000515229.5:n.273A=
ENST00000515425.5:c.3611A=	ENSP00000423660.1:p.Lys1204=
NM_024577.3:c.3611A= , LRG_269t1:c.3611A=	NP_078853.2:p.Lys1204=
NM_024577.4:c.3611A= MANE Select	NP_078853.2:p.Lys1204=