Canonical Allele Identifier: CA361668004

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407620T>C (hg19) ; chr5:g.149028057T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028057T>C , CM000667.2:g.149028057T>C	GRCh38
NC_000005.9:g.148407620T>C , CM000667.1:g.148407620T>C	GRCh37
NC_000005.8:g.148387813T>C	NCBI36
NG_007947.2:g.40118A>G , LRG_269:g.40118A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1571A>G
ENST00000515425.6:c.1675A>G MANE Select	ENSP00000423660.1:p.Asn559Asp
ENST00000675793.1:c.*959A>G	ENSP00000502039.1:n.*959A>G
ENST00000676056.1:c.*1185A>G	ENSP00000501827.1:n.*1185A>G
ENST00000323829.9:c.*1063A>G	ENSP00000313025.5:n.*1063A>G
ENST00000504517.5:c.1205A>G	ENSP00000421779.1:n.1205A>G
ENST00000504690.5:c.1675A>G	ENSP00000425627.1:p.Asn559Asp
ENST00000510779.1:c.725A>G
ENST00000511307.5:c.*1455A>G	ENSP00000421420.1:n.*1455A>G
ENST00000512049.5:c.1654A>G	ENSP00000421860.1:p.Asn552Asp
ENST00000513604.5:c.*1063A>G	ENSP00000423111.1:n.*1063A>G
ENST00000515425.5:c.1675A>G	ENSP00000423660.1:p.Asn559Asp
NM_024577.3:c.1675A>G , LRG_269t1:c.1675A>G	NP_078853.2:p.Asn559Asp
NM_024577.4:c.1675A>G MANE Select	NP_078853.2:p.Asn559Asp