Canonical Allele Identifier: CA361665121

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148406172A>T (hg19) ; chr5:g.149026609A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026609A>T , CM000667.2:g.149026609A>T	GRCh38
NC_000005.9:g.148406172A>T , CM000667.1:g.148406172A>T	GRCh37
NC_000005.8:g.148386365A>T	NCBI36
NG_007947.2:g.41566T>A , LRG_269:g.41566T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2912T>A
ENST00000515425.6:c.3016T>A MANE Select	ENSP00000423660.1:p.Ser1006Thr
ENST00000675793.1:c.*2300T>A	ENSP00000502039.1:n.*2300T>A
ENST00000676056.1:c.*2526T>A	ENSP00000501827.1:n.*2526T>A
ENST00000323829.9:c.*2404T>A	ENSP00000313025.5:n.*2404T>A
ENST00000504517.5:c.2546T>A	ENSP00000421779.1:n.2546T>A
ENST00000504690.5:c.3016T>A	ENSP00000425627.1:p.Ser1006Thr
ENST00000510779.1:c.2066T>A
ENST00000511307.5:c.*2903T>A	ENSP00000421420.1:n.*2903T>A
ENST00000512049.5:c.2995T>A	ENSP00000421860.1:p.Ser999Thr
ENST00000513604.5:c.*2511T>A	ENSP00000423111.1:n.*2511T>A
ENST00000515425.5:c.3016T>A	ENSP00000423660.1:p.Ser1006Thr
NM_024577.3:c.3016T>A , LRG_269t1:c.3016T>A	NP_078853.2:p.Ser1006Thr
NM_024577.4:c.3016T>A MANE Select	NP_078853.2:p.Ser1006Thr