Canonical Allele Identifier: CA515264756
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160632C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722204C>G , CM000684.2:g.50722204C>G GRCh38
NC_000022.10:g.51160632C>G , CM000684.1:g.51160632C>G GRCh37
NC_000022.9:g.49507498C>G NCBI36
NG_008607.2:g.52850C>G
NG_070230.1:g.57988C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3972C>G ENSP00000489147.2:p.Ala1324=
ENST00000414786.7:n.4556C>G
ENST00000445220.7:c.3024C>G ENSP00000489407.2:p.Ala1008=
ENST00000664402.2:c.2514C>G ENSP00000499475.1:p.Ala838=
ENST00000673971.2:c.*2970C>G ENSP00000501192.1:n.*2970C>G
ENST00000445220.6:c.3024C>G ENSP00000489407.2:p.Ala1008=
ENST00000262795.6:c.3972C>G ENSP00000489147.2:p.Ala1324=
ENST00000664402.1:c.2514C>G ENSP00000499475.1:p.Ala838=
ENST00000673971.1:c.*2970C>G ENSP00000501192.1:n.*2970C>G
ENST00000262795.5:c.4368C>G ENSP00000489147.1:p.Ala1456=
ENST00000414786.6:n.4556C>G
ENST00000445220.5:c.4350C>G ENSP00000489407.1:p.Ala1450=