Canonical Allele Identifier: CA515261382
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159609G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721181G>T , CM000684.2:g.50721181G>T GRCh38
NC_000022.10:g.51159609G>T , CM000684.1:g.51159609G>T GRCh37
NC_000022.9:g.49506475G>T NCBI36
NG_008607.2:g.51827G>T
NG_070230.1:g.56965G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2949G>T ENSP00000489147.2:p.Glu983Asp
ENST00000414786.7:n.3533G>T
ENST00000445220.7:c.2001G>T ENSP00000489407.2:p.Glu667Asp
ENST00000664402.2:c.1491G>T ENSP00000499475.1:p.Glu497Asp
ENST00000673971.2:c.*1947G>T ENSP00000501192.1:n.*1947G>T
ENST00000445220.6:c.2001G>T ENSP00000489407.2:p.Glu667Asp
ENST00000262795.6:c.2949G>T ENSP00000489147.2:p.Glu983Asp
ENST00000664402.1:c.1491G>T ENSP00000499475.1:p.Glu497Asp
ENST00000673971.1:c.*1947G>T ENSP00000501192.1:n.*1947G>T
ENST00000262795.5:c.3345G>T ENSP00000489147.1:p.Glu1115Asp
ENST00000414786.6:n.3533G>T
ENST00000445220.5:c.3327G>T ENSP00000489407.1:p.Glu1109Asp