Canonical Allele Identifier: CA447399497

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407309G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027746G>C , CM000667.2:g.149027746G>C	GRCh38
NC_000005.9:g.148407309G>C , CM000667.1:g.148407309G>C	GRCh37
NC_000005.8:g.148387502G>C	NCBI36
NG_007947.2:g.40429C>G , LRG_269:g.40429C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1882C>G
ENST00000515425.6:c.1986C>G MANE Select	ENSP00000423660.1:p.Leu662=
ENST00000675793.1:c.*1270C>G	ENSP00000502039.1:n.*1270C>G
ENST00000676056.1:c.*1496C>G	ENSP00000501827.1:n.*1496C>G
ENST00000323829.9:c.*1374C>G	ENSP00000313025.5:n.*1374C>G
ENST00000504517.5:c.1516C>G	ENSP00000421779.1:n.1516C>G
ENST00000504690.5:c.1986C>G	ENSP00000425627.1:p.Leu662=
ENST00000510779.1:c.1036C>G
ENST00000511307.5:c.*1766C>G	ENSP00000421420.1:n.*1766C>G
ENST00000512049.5:c.1965C>G	ENSP00000421860.1:p.Leu655=
ENST00000513604.5:c.*1374C>G	ENSP00000423111.1:n.*1374C>G
ENST00000515425.5:c.1986C>G	ENSP00000423660.1:p.Leu662=
NM_024577.3:c.1986C>G , LRG_269t1:c.1986C>G	NP_078853.2:p.Leu662=
NM_024577.4:c.1986C>G MANE Select	NP_078853.2:p.Leu662=