Canonical Allele Identifier: CA1590303357

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149006949G= , CM000667.2:g.149006949G=	GRCh38
NC_000005.9:g.148386512G= , CM000667.1:g.148386512G=	GRCh37
NC_000005.8:g.148366705G=	NCBI36
NG_007947.2:g.61226C= , LRG_269:g.61226C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4460C=
ENST00000515425.6:c.3607C= MANE Select	ENSP00000423660.1:p.Pro1203=
ENST00000675793.1:c.*4664C=	ENSP00000502039.1:n.*4664C=
ENST00000323829.9:c.*2995C=	ENSP00000313025.5:n.*2995C=
ENST00000502274.1:c.193C=	ENSP00000421092.1:p.Pro65=
ENST00000504517.5:c.3129C=	ENSP00000421779.1:n.3129C=
ENST00000504690.5:c.3607C=	ENSP00000425627.1:p.Pro1203=
ENST00000510350.1:n.163C=
ENST00000510779.1:c.2657C=
ENST00000512049.5:c.3586C=	ENSP00000421860.1:p.Pro1196=
ENST00000515229.5:n.269C=
ENST00000515425.5:c.3607C=	ENSP00000423660.1:p.Pro1203=
NM_024577.3:c.3607C= , LRG_269t1:c.3607C=	NP_078853.2:p.Pro1203=
NM_024577.4:c.3607C= MANE Select	NP_078853.2:p.Pro1203=