Canonical Allele Identifier: CA515260163
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs2083277686
MyVariant Identifiers: chr22:g.51159172G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720744G>A , CM000684.2:g.50720744G>A GRCh38
NC_000022.10:g.51159172G>A , CM000684.1:g.51159172G>A GRCh37
NC_000022.9:g.49506038G>A NCBI36
NG_008607.2:g.51390G>A
NG_070230.1:g.56528G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2512G>A ENSP00000489147.2:p.Val838Met
ENST00000414786.7:n.3096G>A
ENST00000445220.7:c.1564G>A ENSP00000489407.2:p.Val522Met
ENST00000664402.2:c.1054G>A ENSP00000499475.1:p.Val352Met
ENST00000673971.2:c.*1510G>A ENSP00000501192.1:n.*1510G>A
ENST00000445220.6:c.1564G>A ENSP00000489407.2:p.Val522Met
ENST00000262795.6:c.2512G>A ENSP00000489147.2:p.Val838Met
ENST00000664402.1:c.1054G>A ENSP00000499475.1:p.Val352Met
ENST00000673971.1:c.*1510G>A ENSP00000501192.1:n.*1510G>A
ENST00000262795.5:c.2908G>A ENSP00000489147.1:p.Val970Met
ENST00000414786.6:n.3096G>A
ENST00000445220.5:c.2890G>A ENSP00000489407.1:p.Val964Met