Canonical Allele Identifier: CA3499078
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1982204
ClinVar RCV Id: RCV002766637
dbSNP Id: rs780523281

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149027736G>A , CM000667.2:g.149027736G>A GRCh38
NC_000005.9:g.148407299G>A , CM000667.1:g.148407299G>A GRCh37
NC_000005.8:g.148387492G>A NCBI36
NG_007947.2:g.40439C>T , LRG_269:g.40439C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502274.2:c.1892C>T
ENST00000515425.6:c.1996C>T MANE Select ENSP00000423660.1:p.Pro666Ser
ENST00000675793.1:c.*1280C>T ENSP00000502039.1:n.*1280C>T
ENST00000676056.1:c.*1506C>T ENSP00000501827.1:n.*1506C>T
ENST00000323829.9:c.*1384C>T ENSP00000313025.5:n.*1384C>T
ENST00000504517.5:c.1526C>T ENSP00000421779.1:n.1526C>T
ENST00000504690.5:c.1996C>T ENSP00000425627.1:p.Pro666Ser
ENST00000510779.1:c.1046C>T
ENST00000511307.5:c.*1776C>T ENSP00000421420.1:n.*1776C>T
ENST00000512049.5:c.1975C>T ENSP00000421860.1:p.Pro659Ser
ENST00000513604.5:c.*1384C>T ENSP00000423111.1:n.*1384C>T
ENST00000515425.5:c.1996C>T ENSP00000423660.1:p.Pro666Ser
NM_024577.3:c.1996C>T , LRG_269t1:c.1996C>T NP_078853.2:p.Pro666Ser
NM_024577.4:c.1996C>T MANE Select NP_078853.2:p.Pro666Ser