Canonical Allele Identifier: CA1590304269

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008992C= , CM000667.2:g.149008992C=	GRCh38
NC_000005.9:g.148388555C= , CM000667.1:g.148388555C=	GRCh37
NC_000005.8:g.148368748C=	NCBI36
NG_007947.2:g.59183G= , LRG_269:g.59183G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.3233G=
ENST00000515425.6:c.3337G= MANE Select	ENSP00000423660.1:p.Val1113=
ENST00000675793.1:c.*2621G=	ENSP00000502039.1:n.*2621G=
ENST00000323829.9:c.*2725G=	ENSP00000313025.5:n.*2725G=
ENST00000504517.5:c.2867G=	ENSP00000421779.1:n.2867G=
ENST00000504690.5:c.3337G=	ENSP00000425627.1:p.Val1113=
ENST00000510779.1:c.2387G=
ENST00000512049.5:c.3316G=	ENSP00000421860.1:p.Val1106=
ENST00000515425.5:c.3337G=	ENSP00000423660.1:p.Val1113=
NM_024577.3:c.3337G= , LRG_269t1:c.3337G=	NP_078853.2:p.Val1113=
NM_024577.4:c.3337G= MANE Select	NP_078853.2:p.Val1113=