Canonical Allele Identifier: CA515260607
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159326A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720898A>C , CM000684.2:g.50720898A>C GRCh38
NC_000022.10:g.51159326A>C , CM000684.1:g.51159326A>C GRCh37
NC_000022.9:g.49506192A>C NCBI36
NG_008607.2:g.51544A>C
NG_070230.1:g.56682A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2666A>C ENSP00000489147.2:p.Glu889Ala
ENST00000414786.7:n.3250A>C
ENST00000445220.7:c.1718A>C ENSP00000489407.2:p.Glu573Ala
ENST00000664402.2:c.1208A>C ENSP00000499475.1:p.Glu403Ala
ENST00000673971.2:c.*1664A>C ENSP00000501192.1:n.*1664A>C
ENST00000445220.6:c.1718A>C ENSP00000489407.2:p.Glu573Ala
ENST00000262795.6:c.2666A>C ENSP00000489147.2:p.Glu889Ala
ENST00000664402.1:c.1208A>C ENSP00000499475.1:p.Glu403Ala
ENST00000673971.1:c.*1664A>C ENSP00000501192.1:n.*1664A>C
ENST00000262795.5:c.3062A>C ENSP00000489147.1:p.Glu1021Ala
ENST00000414786.6:n.3250A>C
ENST00000445220.5:c.3044A>C ENSP00000489407.1:p.Glu1015Ala