Canonical Allele Identifier: CA515264693
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160613C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722185C>A , CM000684.2:g.50722185C>A GRCh38
NC_000022.10:g.51160613C>A , CM000684.1:g.51160613C>A GRCh37
NC_000022.9:g.49507479C>A NCBI36
NG_008607.2:g.52831C>A
NG_070230.1:g.57969C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3953C>A ENSP00000489147.2:p.Ser1318Tyr
ENST00000414786.7:n.4537C>A
ENST00000445220.7:c.3005C>A ENSP00000489407.2:p.Ser1002Tyr
ENST00000664402.2:c.2495C>A ENSP00000499475.1:p.Ser832Tyr
ENST00000673971.2:c.*2951C>A ENSP00000501192.1:n.*2951C>A
ENST00000445220.6:c.3005C>A ENSP00000489407.2:p.Ser1002Tyr
ENST00000262795.6:c.3953C>A ENSP00000489147.2:p.Ser1318Tyr
ENST00000664402.1:c.2495C>A ENSP00000499475.1:p.Ser832Tyr
ENST00000673971.1:c.*2951C>A ENSP00000501192.1:n.*2951C>A
ENST00000262795.5:c.4349C>A ENSP00000489147.1:p.Ser1450Tyr
ENST00000414786.6:n.4537C>A
ENST00000445220.5:c.4331C>A ENSP00000489407.1:p.Ser1444Tyr