Canonical Allele Identifier: CA515264912
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160682G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722254G>A , CM000684.2:g.50722254G>A GRCh38
NC_000022.10:g.51160682G>A , CM000684.1:g.51160682G>A GRCh37
NC_000022.9:g.49507548G>A NCBI36
NG_008607.2:g.52900G>A
NG_070230.1:g.58038G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4022G>A ENSP00000489147.2:p.Trp1341Ter
ENST00000414786.7:n.4606G>A
ENST00000445220.7:c.3074G>A ENSP00000489407.2:p.Trp1025Ter
ENST00000664402.2:c.2564G>A ENSP00000499475.1:p.Trp855Ter
ENST00000673971.2:c.*3020G>A ENSP00000501192.1:n.*3020G>A
ENST00000445220.6:c.3074G>A ENSP00000489407.2:p.Trp1025Ter
ENST00000262795.6:c.4022G>A ENSP00000489147.2:p.Trp1341Ter
ENST00000664402.1:c.2564G>A ENSP00000499475.1:p.Trp855Ter
ENST00000673971.1:c.*3020G>A ENSP00000501192.1:n.*3020G>A
ENST00000262795.5:c.4418G>A ENSP00000489147.1:p.Trp1473Ter
ENST00000414786.6:n.4606G>A
ENST00000445220.5:c.4400G>A ENSP00000489407.1:p.Trp1467Ter