Canonical Allele Identifier: CA361667885

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028020A>G , CM000667.2:g.149028020A>G	GRCh38
NC_000005.9:g.148407583A>G , CM000667.1:g.148407583A>G	GRCh37
NC_000005.8:g.148387776A>G	NCBI36
NG_007947.2:g.40155T>C , LRG_269:g.40155T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024577.4:c.1712T>C MANE Select	NP_078853.2:p.Leu571Pro
ENST00000515425.6:c.1712T>C MANE Select	ENSP00000423660.1:p.Leu571Pro
NM_024577.3:c.1712T>C , LRG_269t1:c.1712T>C	NP_078853.2:p.Leu571Pro
ENST00000323829.9:c.*1100T>C	ENSP00000313025.5:n.*1100T>C
ENST00000502274.2:c.1608T>C
ENST00000504517.5:c.1242T>C	ENSP00000421779.1:n.1242T>C
ENST00000504690.5:c.1712T>C	ENSP00000425627.1:p.Leu571Pro
ENST00000510779.1:c.762T>C
ENST00000511307.5:c.*1492T>C	ENSP00000421420.1:n.*1492T>C
ENST00000512049.5:c.1691T>C	ENSP00000421860.1:p.Leu564Pro
ENST00000513604.5:c.*1100T>C	ENSP00000423111.1:n.*1100T>C
ENST00000515425.5:c.1712T>C	ENSP00000423660.1:p.Leu571Pro
ENST00000675793.1:c.*996T>C	ENSP00000502039.1:n.*996T>C
ENST00000676056.1:c.*1222T>C	ENSP00000501827.1:n.*1222T>C