Canonical Allele Identifier: CA515263675
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160275A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721847A>T , CM000684.2:g.50721847A>T GRCh38
NC_000022.10:g.51160275A>T , CM000684.1:g.51160275A>T GRCh37
NC_000022.9:g.49507141A>T NCBI36
NG_008607.2:g.52493A>T
NG_070230.1:g.57631A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3615A>T ENSP00000489147.2:p.Ser1205=
ENST00000414786.7:n.4199A>T
ENST00000445220.7:c.2667A>T ENSP00000489407.2:p.Ser889=
ENST00000664402.2:c.2157A>T ENSP00000499475.1:p.Ser719=
ENST00000673971.2:c.*2613A>T ENSP00000501192.1:n.*2613A>T
ENST00000445220.6:c.2667A>T ENSP00000489407.2:p.Ser889=
ENST00000262795.6:c.3615A>T ENSP00000489147.2:p.Ser1205=
ENST00000664402.1:c.2157A>T ENSP00000499475.1:p.Ser719=
ENST00000673971.1:c.*2613A>T ENSP00000501192.1:n.*2613A>T
ENST00000262795.5:c.4011A>T ENSP00000489147.1:p.Ser1337=
ENST00000414786.6:n.4199A>T
ENST00000445220.5:c.3993A>T ENSP00000489407.1:p.Ser1331=