Canonical Allele Identifier: CA515263261
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160135T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721707T>A , CM000684.2:g.50721707T>A GRCh38
NC_000022.10:g.51160135T>A , CM000684.1:g.51160135T>A GRCh37
NC_000022.9:g.49507001T>A NCBI36
NG_008607.2:g.52353T>A
NG_070230.1:g.57491T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3475T>A ENSP00000489147.2:p.Ser1159Thr
ENST00000414786.7:n.4059T>A
ENST00000445220.7:c.2527T>A ENSP00000489407.2:p.Ser843Thr
ENST00000664402.2:c.2017T>A ENSP00000499475.1:p.Ser673Thr
ENST00000673971.2:c.*2473T>A ENSP00000501192.1:n.*2473T>A
ENST00000445220.6:c.2527T>A ENSP00000489407.2:p.Ser843Thr
ENST00000262795.6:c.3475T>A ENSP00000489147.2:p.Ser1159Thr
ENST00000664402.1:c.2017T>A ENSP00000499475.1:p.Ser673Thr
ENST00000673971.1:c.*2473T>A ENSP00000501192.1:n.*2473T>A
ENST00000262795.5:c.3871T>A ENSP00000489147.1:p.Ser1291Thr
ENST00000414786.6:n.4059T>A
ENST00000445220.5:c.3853T>A ENSP00000489407.1:p.Ser1285Thr