Canonical Allele Identifier: CA361667982

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407610A>T (hg19) ; chr5:g.149028047A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028047A>T , CM000667.2:g.149028047A>T	GRCh38
NC_000005.9:g.148407610A>T , CM000667.1:g.148407610A>T	GRCh37
NC_000005.8:g.148387803A>T	NCBI36
NG_007947.2:g.40128T>A , LRG_269:g.40128T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1581T>A
ENST00000515425.6:c.1685T>A MANE Select	ENSP00000423660.1:p.Phe562Tyr
ENST00000675793.1:c.*969T>A	ENSP00000502039.1:n.*969T>A
ENST00000676056.1:c.*1195T>A	ENSP00000501827.1:n.*1195T>A
ENST00000323829.9:c.*1073T>A	ENSP00000313025.5:n.*1073T>A
ENST00000504517.5:c.1215T>A	ENSP00000421779.1:n.1215T>A
ENST00000504690.5:c.1685T>A	ENSP00000425627.1:p.Phe562Tyr
ENST00000510779.1:c.735T>A
ENST00000511307.5:c.*1465T>A	ENSP00000421420.1:n.*1465T>A
ENST00000512049.5:c.1664T>A	ENSP00000421860.1:p.Phe555Tyr
ENST00000513604.5:c.*1073T>A	ENSP00000423111.1:n.*1073T>A
ENST00000515425.5:c.1685T>A	ENSP00000423660.1:p.Phe562Tyr
NM_024577.3:c.1685T>A , LRG_269t1:c.1685T>A	NP_078853.2:p.Phe562Tyr
NM_024577.4:c.1685T>A MANE Select	NP_078853.2:p.Phe562Tyr