Canonical Allele Identifier: CA447399614

Gene: SH3TC2

Linked Data

• COSMIC: COSM5647911 ; COSM5647912
• MyVariant Identifiers: chr5:g.148407621G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028058G>C , CM000667.2:g.149028058G>C	GRCh38
NC_000005.9:g.148407621G>C , CM000667.1:g.148407621G>C	GRCh37
NC_000005.8:g.148387814G>C	NCBI36
NG_007947.2:g.40117C>G , LRG_269:g.40117C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1570C>G
ENST00000515425.6:c.1674C>G MANE Select	ENSP00000423660.1:p.Leu558=
ENST00000675793.1:c.*958C>G	ENSP00000502039.1:n.*958C>G
ENST00000676056.1:c.*1184C>G	ENSP00000501827.1:n.*1184C>G
ENST00000323829.9:c.*1062C>G	ENSP00000313025.5:n.*1062C>G
ENST00000504517.5:c.1204C>G	ENSP00000421779.1:n.1204C>G
ENST00000504690.5:c.1674C>G	ENSP00000425627.1:p.Leu558=
ENST00000510779.1:c.724C>G
ENST00000511307.5:c.*1454C>G	ENSP00000421420.1:n.*1454C>G
ENST00000512049.5:c.1653C>G	ENSP00000421860.1:p.Leu551=
ENST00000513604.5:c.*1062C>G	ENSP00000423111.1:n.*1062C>G
ENST00000515425.5:c.1674C>G	ENSP00000423660.1:p.Leu558=
NM_024577.3:c.1674C>G , LRG_269t1:c.1674C>G	NP_078853.2:p.Leu558=
NM_024577.4:c.1674C>G MANE Select	NP_078853.2:p.Leu558=