Canonical Allele Identifier: CA515263974
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160366C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721938C>G , CM000684.2:g.50721938C>G GRCh38
NC_000022.10:g.51160366C>G , CM000684.1:g.51160366C>G GRCh37
NC_000022.9:g.49507232C>G NCBI36
NG_008607.2:g.52584C>G
NG_070230.1:g.57722C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3706C>G ENSP00000489147.2:p.His1236Asp
ENST00000414786.7:n.4290C>G
ENST00000445220.7:c.2758C>G ENSP00000489407.2:p.His920Asp
ENST00000664402.2:c.2248C>G ENSP00000499475.1:p.His750Asp
ENST00000673971.2:c.*2704C>G ENSP00000501192.1:n.*2704C>G
ENST00000445220.6:c.2758C>G ENSP00000489407.2:p.His920Asp
ENST00000262795.6:c.3706C>G ENSP00000489147.2:p.His1236Asp
ENST00000664402.1:c.2248C>G ENSP00000499475.1:p.His750Asp
ENST00000673971.1:c.*2704C>G ENSP00000501192.1:n.*2704C>G
ENST00000262795.5:c.4102C>G ENSP00000489147.1:p.His1368Asp
ENST00000414786.6:n.4290C>G
ENST00000445220.5:c.4084C>G ENSP00000489407.1:p.His1362Asp