Canonical Allele Identifier: CA515263557
Gene: SHANK3 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3575G>C ENSP00000489147.2:p.Gly1192Ala
ENST00000414786.7:n.4159G>C
ENST00000445220.7:c.2627G>C ENSP00000489407.2:p.Gly876Ala
ENST00000664402.2:c.2117G>C ENSP00000499475.1:p.Gly706Ala
ENST00000673971.2:c.*2573G>C ENSP00000501192.1:n.*2573G>C
ENST00000445220.6:c.2627G>C ENSP00000489407.2:p.Gly876Ala
ENST00000262795.6:c.3575G>C ENSP00000489147.2:p.Gly1192Ala
ENST00000664402.1:c.2117G>C ENSP00000499475.1:p.Gly706Ala
ENST00000673971.1:c.*2573G>C ENSP00000501192.1:n.*2573G>C
ENST00000262795.5:c.3971G>C ENSP00000489147.1:p.Gly1324Ala
ENST00000414786.6:n.4159G>C
ENST00000445220.5:c.3953G>C ENSP00000489407.1:p.Gly1318Ala