Canonical Allele Identifier: CA361667435

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407367A>T (hg19) ; chr5:g.149027804A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027804A>T , CM000667.2:g.149027804A>T	GRCh38
NC_000005.9:g.148407367A>T , CM000667.1:g.148407367A>T	GRCh37
NC_000005.8:g.148387560A>T	NCBI36
NG_007947.2:g.40371T>A , LRG_269:g.40371T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1824T>A
ENST00000515425.6:c.1928T>A MANE Select	ENSP00000423660.1:p.Leu643His
ENST00000675793.1:c.*1212T>A	ENSP00000502039.1:n.*1212T>A
ENST00000676056.1:c.*1438T>A	ENSP00000501827.1:n.*1438T>A
ENST00000323829.9:c.*1316T>A	ENSP00000313025.5:n.*1316T>A
ENST00000504517.5:c.1458T>A	ENSP00000421779.1:n.1458T>A
ENST00000504690.5:c.1928T>A	ENSP00000425627.1:p.Leu643His
ENST00000510779.1:c.978T>A
ENST00000511307.5:c.*1708T>A	ENSP00000421420.1:n.*1708T>A
ENST00000512049.5:c.1907T>A	ENSP00000421860.1:p.Leu636His
ENST00000513604.5:c.*1316T>A	ENSP00000423111.1:n.*1316T>A
ENST00000515425.5:c.1928T>A	ENSP00000423660.1:p.Leu643His
NM_024577.3:c.1928T>A , LRG_269t1:c.1928T>A	NP_078853.2:p.Leu643His
NM_024577.4:c.1928T>A MANE Select	NP_078853.2:p.Leu643His