Canonical Allele Identifier: CA515263503
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160220C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721792C>G , CM000684.2:g.50721792C>G GRCh38
NC_000022.10:g.51160220C>G , CM000684.1:g.51160220C>G GRCh37
NC_000022.9:g.49507086C>G NCBI36
NG_008607.2:g.52438C>G
NG_070230.1:g.57576C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3560C>G ENSP00000489147.2:p.Ala1187Gly
ENST00000414786.7:n.4144C>G
ENST00000445220.7:c.2612C>G ENSP00000489407.2:p.Ala871Gly
ENST00000664402.2:c.2102C>G ENSP00000499475.1:p.Ala701Gly
ENST00000673971.2:c.*2558C>G ENSP00000501192.1:n.*2558C>G
ENST00000445220.6:c.2612C>G ENSP00000489407.2:p.Ala871Gly
ENST00000262795.6:c.3560C>G ENSP00000489147.2:p.Ala1187Gly
ENST00000664402.1:c.2102C>G ENSP00000499475.1:p.Ala701Gly
ENST00000673971.1:c.*2558C>G ENSP00000501192.1:n.*2558C>G
ENST00000262795.5:c.3956C>G ENSP00000489147.1:p.Ala1319Gly
ENST00000414786.6:n.4144C>G
ENST00000445220.5:c.3938C>G ENSP00000489407.1:p.Ala1313Gly