Canonical Allele Identifier: CA3499047

Gene: SH3TC2

Linked Data

• dbSNP Id: rs762180141
• ExAC: 5:148407110 A / C
• gnomAD v2: 5-148407110-A-C
• MyVariant Identifiers: chr5:g.148407110A>C (hg19) ; chr5:g.149027547A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027547A>C , CM000667.2:g.149027547A>C	GRCh38
NC_000005.9:g.148407110A>C , CM000667.1:g.148407110A>C	GRCh37
NC_000005.8:g.148387303A>C	NCBI36
NG_007947.2:g.40628T>G , LRG_269:g.40628T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.2081T>G
ENST00000515425.6:c.2185T>G MANE Select	ENSP00000423660.1:p.Trp729Gly
ENST00000675793.1:c.*1469T>G	ENSP00000502039.1:n.*1469T>G
ENST00000676056.1:c.*1695T>G	ENSP00000501827.1:n.*1695T>G
ENST00000323829.9:c.*1573T>G	ENSP00000313025.5:n.*1573T>G
ENST00000504517.5:c.1715T>G	ENSP00000421779.1:n.1715T>G
ENST00000504690.5:c.2185T>G	ENSP00000425627.1:p.Trp729Gly
ENST00000510779.1:c.1235T>G
ENST00000511307.5:c.*1965T>G	ENSP00000421420.1:n.*1965T>G
ENST00000512049.5:c.2164T>G	ENSP00000421860.1:p.Trp722Gly
ENST00000513604.5:c.*1573T>G	ENSP00000423111.1:n.*1573T>G
ENST00000515425.5:c.2185T>G	ENSP00000423660.1:p.Trp729Gly
NM_024577.3:c.2185T>G , LRG_269t1:c.2185T>G	NP_078853.2:p.Trp729Gly
NM_024577.4:c.2185T>G MANE Select	NP_078853.2:p.Trp729Gly