Canonical Allele Identifier: CA361667228

Gene: SH3TC2

Linked Data

• dbSNP Id: rs1754096404
• MyVariant Identifiers: chr5:g.148407264A>T (hg19) ; chr5:g.149027701A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027701A>T , CM000667.2:g.149027701A>T	GRCh38
NC_000005.9:g.148407264A>T , CM000667.1:g.148407264A>T	GRCh37
NC_000005.8:g.148387457A>T	NCBI36
NG_007947.2:g.40474T>A , LRG_269:g.40474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1927T>A
ENST00000515425.6:c.2031T>A MANE Select	ENSP00000423660.1:p.Ser677Arg
ENST00000675793.1:c.*1315T>A	ENSP00000502039.1:n.*1315T>A
ENST00000676056.1:c.*1541T>A	ENSP00000501827.1:n.*1541T>A
ENST00000323829.9:c.*1419T>A	ENSP00000313025.5:n.*1419T>A
ENST00000504517.5:c.1561T>A	ENSP00000421779.1:n.1561T>A
ENST00000504690.5:c.2031T>A	ENSP00000425627.1:p.Ser677Arg
ENST00000510779.1:c.1081T>A
ENST00000511307.5:c.*1811T>A	ENSP00000421420.1:n.*1811T>A
ENST00000512049.5:c.2010T>A	ENSP00000421860.1:p.Ser670Arg
ENST00000513604.5:c.*1419T>A	ENSP00000423111.1:n.*1419T>A
ENST00000515425.5:c.2031T>A	ENSP00000423660.1:p.Ser677Arg
NM_024577.3:c.2031T>A , LRG_269t1:c.2031T>A	NP_078853.2:p.Ser677Arg
NM_024577.4:c.2031T>A MANE Select	NP_078853.2:p.Ser677Arg