Canonical Allele Identifier: CA515259926
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159089C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720661C>A , CM000684.2:g.50720661C>A GRCh38
NC_000022.10:g.51159089C>A , CM000684.1:g.51159089C>A GRCh37
NC_000022.9:g.49505955C>A NCBI36
NG_008607.2:g.51307C>A
NG_070230.1:g.56445C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2429C>A ENSP00000489147.2:p.Ala810Asp
ENST00000414786.7:n.3013C>A
ENST00000445220.7:c.1481C>A ENSP00000489407.2:p.Ala494Asp
ENST00000664402.2:c.971C>A ENSP00000499475.1:p.Ala324Asp
ENST00000673971.2:c.*1427C>A ENSP00000501192.1:n.*1427C>A
ENST00000445220.6:c.1481C>A ENSP00000489407.2:p.Ala494Asp
ENST00000262795.6:c.2429C>A ENSP00000489147.2:p.Ala810Asp
ENST00000664402.1:c.971C>A ENSP00000499475.1:p.Ala324Asp
ENST00000673971.1:c.*1427C>A ENSP00000501192.1:n.*1427C>A
ENST00000262795.5:c.2825C>A ENSP00000489147.1:p.Ala942Asp
ENST00000414786.6:n.3013C>A
ENST00000445220.5:c.2807C>A ENSP00000489407.1:p.Ala936Asp