Canonical Allele Identifier: CA515259260
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51158863G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720435G>A , CM000684.2:g.50720435G>A GRCh38
NC_000022.10:g.51158863G>A , CM000684.1:g.51158863G>A GRCh37
NC_000022.9:g.49505729G>A NCBI36
NG_008607.2:g.51081G>A
NG_070230.1:g.56219G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2203G>A ENSP00000489147.2:p.Ala735Thr
ENST00000414786.7:n.2787G>A
ENST00000445220.7:c.1255G>A ENSP00000489407.2:p.Ala419Thr
ENST00000664402.2:c.745G>A ENSP00000499475.1:p.Ala249Thr
ENST00000673971.2:c.*1201G>A ENSP00000501192.1:n.*1201G>A
ENST00000445220.6:c.1255G>A ENSP00000489407.2:p.Ala419Thr
ENST00000262795.6:c.2203G>A ENSP00000489147.2:p.Ala735Thr
ENST00000664402.1:c.745G>A ENSP00000499475.1:p.Ala249Thr
ENST00000673971.1:c.*1201G>A ENSP00000501192.1:n.*1201G>A
ENST00000262795.5:c.2599G>A ENSP00000489147.1:p.Ala867Thr
ENST00000414786.6:n.2787G>A
ENST00000445220.5:c.2581G>A ENSP00000489407.1:p.Ala861Thr