Canonical Allele Identifier: CA515264759
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160634C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722206C>A , CM000684.2:g.50722206C>A GRCh38
NC_000022.10:g.51160634C>A , CM000684.1:g.51160634C>A GRCh37
NC_000022.9:g.49507500C>A NCBI36
NG_008607.2:g.52852C>A
NG_070230.1:g.57990C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3974C>A ENSP00000489147.2:p.Ala1325Asp
ENST00000414786.7:n.4558C>A
ENST00000445220.7:c.3026C>A ENSP00000489407.2:p.Ala1009Asp
ENST00000664402.2:c.2516C>A ENSP00000499475.1:p.Ala839Asp
ENST00000673971.2:c.*2972C>A ENSP00000501192.1:n.*2972C>A
ENST00000445220.6:c.3026C>A ENSP00000489407.2:p.Ala1009Asp
ENST00000262795.6:c.3974C>A ENSP00000489147.2:p.Ala1325Asp
ENST00000664402.1:c.2516C>A ENSP00000499475.1:p.Ala839Asp
ENST00000673971.1:c.*2972C>A ENSP00000501192.1:n.*2972C>A
ENST00000262795.5:c.4370C>A ENSP00000489147.1:p.Ala1457Asp
ENST00000414786.6:n.4558C>A
ENST00000445220.5:c.4352C>A ENSP00000489407.1:p.Ala1451Asp