Canonical Allele Identifier: CA515261367
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159604C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721176C>G , CM000684.2:g.50721176C>G GRCh38
NC_000022.10:g.51159604C>G , CM000684.1:g.51159604C>G GRCh37
NC_000022.9:g.49506470C>G NCBI36
NG_008607.2:g.51822C>G
NG_070230.1:g.56960C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2944C>G ENSP00000489147.2:p.Arg982Gly
ENST00000414786.7:n.3528C>G
ENST00000445220.7:c.1996C>G ENSP00000489407.2:p.Arg666Gly
ENST00000664402.2:c.1486C>G ENSP00000499475.1:p.Arg496Gly
ENST00000673971.2:c.*1942C>G ENSP00000501192.1:n.*1942C>G
ENST00000445220.6:c.1996C>G ENSP00000489407.2:p.Arg666Gly
ENST00000262795.6:c.2944C>G ENSP00000489147.2:p.Arg982Gly
ENST00000664402.1:c.1486C>G ENSP00000499475.1:p.Arg496Gly
ENST00000673971.1:c.*1942C>G ENSP00000501192.1:n.*1942C>G
ENST00000262795.5:c.3340C>G ENSP00000489147.1:p.Arg1114Gly
ENST00000414786.6:n.3528C>G
ENST00000445220.5:c.3322C>G ENSP00000489407.1:p.Arg1108Gly