Canonical Allele Identifier: CA515260619
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159330G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720902G>C , CM000684.2:g.50720902G>C GRCh38
NC_000022.10:g.51159330G>C , CM000684.1:g.51159330G>C GRCh37
NC_000022.9:g.49506196G>C NCBI36
NG_008607.2:g.51548G>C
NG_070230.1:g.56686G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2670G>C ENSP00000489147.2:p.Arg890=
ENST00000414786.7:n.3254G>C
ENST00000445220.7:c.1722G>C ENSP00000489407.2:p.Arg574=
ENST00000664402.2:c.1212G>C ENSP00000499475.1:p.Arg404=
ENST00000673971.2:c.*1668G>C ENSP00000501192.1:n.*1668G>C
ENST00000445220.6:c.1722G>C ENSP00000489407.2:p.Arg574=
ENST00000262795.6:c.2670G>C ENSP00000489147.2:p.Arg890=
ENST00000664402.1:c.1212G>C ENSP00000499475.1:p.Arg404=
ENST00000673971.1:c.*1668G>C ENSP00000501192.1:n.*1668G>C
ENST00000262795.5:c.3066G>C ENSP00000489147.1:p.Arg1022=
ENST00000414786.6:n.3254G>C
ENST00000445220.5:c.3048G>C ENSP00000489407.1:p.Arg1016=