Canonical Allele Identifier: CA361667326

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407311G>C (hg19) ; chr5:g.149027748G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027748G>C , CM000667.2:g.149027748G>C	GRCh38
NC_000005.9:g.148407311G>C , CM000667.1:g.148407311G>C	GRCh37
NC_000005.8:g.148387504G>C	NCBI36
NG_007947.2:g.40427C>G , LRG_269:g.40427C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1880C>G
ENST00000515425.6:c.1984C>G MANE Select	ENSP00000423660.1:p.Leu662Val
ENST00000675793.1:c.*1268C>G	ENSP00000502039.1:n.*1268C>G
ENST00000676056.1:c.*1494C>G	ENSP00000501827.1:n.*1494C>G
ENST00000323829.9:c.*1372C>G	ENSP00000313025.5:n.*1372C>G
ENST00000504517.5:c.1514C>G	ENSP00000421779.1:n.1514C>G
ENST00000504690.5:c.1984C>G	ENSP00000425627.1:p.Leu662Val
ENST00000510779.1:c.1034C>G
ENST00000511307.5:c.*1764C>G	ENSP00000421420.1:n.*1764C>G
ENST00000512049.5:c.1963C>G	ENSP00000421860.1:p.Leu655Val
ENST00000513604.5:c.*1372C>G	ENSP00000423111.1:n.*1372C>G
ENST00000515425.5:c.1984C>G	ENSP00000423660.1:p.Leu662Val
NM_024577.3:c.1984C>G , LRG_269t1:c.1984C>G	NP_078853.2:p.Leu662Val
NM_024577.4:c.1984C>G MANE Select	NP_078853.2:p.Leu662Val