Canonical Allele Identifier: CA515263558
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160235G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721807G>T , CM000684.2:g.50721807G>T GRCh38
NC_000022.10:g.51160235G>T , CM000684.1:g.51160235G>T GRCh37
NC_000022.9:g.49507101G>T NCBI36
NG_008607.2:g.52453G>T
NG_070230.1:g.57591G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3575G>T ENSP00000489147.2:p.Gly1192Val
ENST00000414786.7:n.4159G>T
ENST00000445220.7:c.2627G>T ENSP00000489407.2:p.Gly876Val
ENST00000664402.2:c.2117G>T ENSP00000499475.1:p.Gly706Val
ENST00000673971.2:c.*2573G>T ENSP00000501192.1:n.*2573G>T
ENST00000445220.6:c.2627G>T ENSP00000489407.2:p.Gly876Val
ENST00000262795.6:c.3575G>T ENSP00000489147.2:p.Gly1192Val
ENST00000664402.1:c.2117G>T ENSP00000499475.1:p.Gly706Val
ENST00000673971.1:c.*2573G>T ENSP00000501192.1:n.*2573G>T
ENST00000262795.5:c.3971G>T ENSP00000489147.1:p.Gly1324Val
ENST00000414786.6:n.4159G>T
ENST00000445220.5:c.3953G>T ENSP00000489407.1:p.Gly1318Val