Canonical Allele Identifier: CA515264408
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160520C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722092C>G , CM000684.2:g.50722092C>G GRCh38
NC_000022.10:g.51160520C>G , CM000684.1:g.51160520C>G GRCh37
NC_000022.9:g.49507386C>G NCBI36
NG_008607.2:g.52738C>G
NG_070230.1:g.57876C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3860C>G ENSP00000489147.2:p.Ser1287Cys
ENST00000414786.7:n.4444C>G
ENST00000445220.7:c.2912C>G ENSP00000489407.2:p.Ser971Cys
ENST00000664402.2:c.2402C>G ENSP00000499475.1:p.Ser801Cys
ENST00000673971.2:c.*2858C>G ENSP00000501192.1:n.*2858C>G
ENST00000445220.6:c.2912C>G ENSP00000489407.2:p.Ser971Cys
ENST00000262795.6:c.3860C>G ENSP00000489147.2:p.Ser1287Cys
ENST00000664402.1:c.2402C>G ENSP00000499475.1:p.Ser801Cys
ENST00000673971.1:c.*2858C>G ENSP00000501192.1:n.*2858C>G
ENST00000262795.5:c.4256C>G ENSP00000489147.1:p.Ser1419Cys
ENST00000414786.6:n.4444C>G
ENST00000445220.5:c.4238C>G ENSP00000489407.1:p.Ser1413Cys