Canonical Allele Identifier: CA515263954
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160359C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721931C>G , CM000684.2:g.50721931C>G GRCh38
NC_000022.10:g.51160359C>G , CM000684.1:g.51160359C>G GRCh37
NC_000022.9:g.49507225C>G NCBI36
NG_008607.2:g.52577C>G
NG_070230.1:g.57715C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3699C>G ENSP00000489147.2:p.Ser1233Arg
ENST00000414786.7:n.4283C>G
ENST00000445220.7:c.2751C>G ENSP00000489407.2:p.Ser917Arg
ENST00000664402.2:c.2241C>G ENSP00000499475.1:p.Ser747Arg
ENST00000673971.2:c.*2697C>G ENSP00000501192.1:n.*2697C>G
ENST00000445220.6:c.2751C>G ENSP00000489407.2:p.Ser917Arg
ENST00000262795.6:c.3699C>G ENSP00000489147.2:p.Ser1233Arg
ENST00000664402.1:c.2241C>G ENSP00000499475.1:p.Ser747Arg
ENST00000673971.1:c.*2697C>G ENSP00000501192.1:n.*2697C>G
ENST00000262795.5:c.4095C>G ENSP00000489147.1:p.Ser1365Arg
ENST00000414786.6:n.4283C>G
ENST00000445220.5:c.4077C>G ENSP00000489407.1:p.Ser1359Arg