Canonical Allele Identifier: CA515264787
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160642G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722214G>A , CM000684.2:g.50722214G>A GRCh38
NC_000022.10:g.51160642G>A , CM000684.1:g.51160642G>A GRCh37
NC_000022.9:g.49507508G>A NCBI36
NG_008607.2:g.52860G>A
NG_070230.1:g.57998G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3982G>A ENSP00000489147.2:p.Ala1328Thr
ENST00000414786.7:n.4566G>A
ENST00000445220.7:c.3034G>A ENSP00000489407.2:p.Ala1012Thr
ENST00000664402.2:c.2524G>A ENSP00000499475.1:p.Ala842Thr
ENST00000673971.2:c.*2980G>A ENSP00000501192.1:n.*2980G>A
ENST00000445220.6:c.3034G>A ENSP00000489407.2:p.Ala1012Thr
ENST00000262795.6:c.3982G>A ENSP00000489147.2:p.Ala1328Thr
ENST00000664402.1:c.2524G>A ENSP00000499475.1:p.Ala842Thr
ENST00000673971.1:c.*2980G>A ENSP00000501192.1:n.*2980G>A
ENST00000262795.5:c.4378G>A ENSP00000489147.1:p.Ala1460Thr
ENST00000414786.6:n.4566G>A
ENST00000445220.5:c.4360G>A ENSP00000489407.1:p.Ala1454Thr