Canonical Allele Identifier: CA515260728
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159369G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720941G>T , CM000684.2:g.50720941G>T GRCh38
NC_000022.10:g.51159369G>T , CM000684.1:g.51159369G>T GRCh37
NC_000022.9:g.49506235G>T NCBI36
NG_008607.2:g.51587G>T
NG_070230.1:g.56725G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2709G>T ENSP00000489147.2:p.Glu903Asp
ENST00000414786.7:n.3293G>T
ENST00000445220.7:c.1761G>T ENSP00000489407.2:p.Glu587Asp
ENST00000664402.2:c.1251G>T ENSP00000499475.1:p.Glu417Asp
ENST00000673971.2:c.*1707G>T ENSP00000501192.1:n.*1707G>T
ENST00000445220.6:c.1761G>T ENSP00000489407.2:p.Glu587Asp
ENST00000262795.6:c.2709G>T ENSP00000489147.2:p.Glu903Asp
ENST00000664402.1:c.1251G>T ENSP00000499475.1:p.Glu417Asp
ENST00000673971.1:c.*1707G>T ENSP00000501192.1:n.*1707G>T
ENST00000262795.5:c.3105G>T ENSP00000489147.1:p.Glu1035Asp
ENST00000414786.6:n.3293G>T
ENST00000445220.5:c.3087G>T ENSP00000489407.1:p.Glu1029Asp