Canonical Allele Identifier: CA447398207

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148406435G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026872G>T , CM000667.2:g.149026872G>T	GRCh38
NC_000005.9:g.148406435G>T , CM000667.1:g.148406435G>T	GRCh37
NC_000005.8:g.148386628G>T	NCBI36
NG_007947.2:g.41303C>A , LRG_269:g.41303C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2756C>A
ENST00000515425.6:c.2860C>A MANE Select	ENSP00000423660.1:p.Arg954=
ENST00000675793.1:c.*2144C>A	ENSP00000502039.1:n.*2144C>A
ENST00000676056.1:c.*2370C>A	ENSP00000501827.1:n.*2370C>A
ENST00000323829.9:c.*2248C>A	ENSP00000313025.5:n.*2248C>A
ENST00000504517.5:c.2390C>A	ENSP00000421779.1:n.2390C>A
ENST00000504690.5:c.2860C>A	ENSP00000425627.1:p.Arg954=
ENST00000510779.1:c.1910C>A
ENST00000511307.5:c.*2640C>A	ENSP00000421420.1:n.*2640C>A
ENST00000512049.5:c.2839C>A	ENSP00000421860.1:p.Arg947=
ENST00000513604.5:c.*2248C>A	ENSP00000423111.1:n.*2248C>A
ENST00000515425.5:c.2860C>A	ENSP00000423660.1:p.Arg954=
NM_024577.3:c.2860C>A , LRG_269t1:c.2860C>A	NP_078853.2:p.Arg954=
NM_024577.4:c.2860C>A MANE Select	NP_078853.2:p.Arg954=