Canonical Allele Identifier: CA515261389
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159612A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721184A>T , CM000684.2:g.50721184A>T GRCh38
NC_000022.10:g.51159612A>T , CM000684.1:g.51159612A>T GRCh37
NC_000022.9:g.49506478A>T NCBI36
NG_008607.2:g.51830A>T
NG_070230.1:g.56968A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2952A>T ENSP00000489147.2:p.Arg984=
ENST00000414786.7:n.3536A>T
ENST00000445220.7:c.2004A>T ENSP00000489407.2:p.Arg668=
ENST00000664402.2:c.1494A>T ENSP00000499475.1:p.Arg498=
ENST00000673971.2:c.*1950A>T ENSP00000501192.1:n.*1950A>T
ENST00000445220.6:c.2004A>T ENSP00000489407.2:p.Arg668=
ENST00000262795.6:c.2952A>T ENSP00000489147.2:p.Arg984=
ENST00000664402.1:c.1494A>T ENSP00000499475.1:p.Arg498=
ENST00000673971.1:c.*1950A>T ENSP00000501192.1:n.*1950A>T
ENST00000262795.5:c.3348A>T ENSP00000489147.1:p.Arg1116=
ENST00000414786.6:n.3536A>T
ENST00000445220.5:c.3330A>T ENSP00000489407.1:p.Arg1110=