Canonical Allele Identifier: CA515260969
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159460G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721032G>C , CM000684.2:g.50721032G>C GRCh38
NC_000022.10:g.51159460G>C , CM000684.1:g.51159460G>C GRCh37
NC_000022.9:g.49506326G>C NCBI36
NG_008607.2:g.51678G>C
NG_070230.1:g.56816G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2800G>C ENSP00000489147.2:p.Asp934His
ENST00000414786.7:n.3384G>C
ENST00000445220.7:c.1852G>C ENSP00000489407.2:p.Asp618His
ENST00000664402.2:c.1342G>C ENSP00000499475.1:p.Asp448His
ENST00000673971.2:c.*1798G>C ENSP00000501192.1:n.*1798G>C
ENST00000445220.6:c.1852G>C ENSP00000489407.2:p.Asp618His
ENST00000262795.6:c.2800G>C ENSP00000489147.2:p.Asp934His
ENST00000664402.1:c.1342G>C ENSP00000499475.1:p.Asp448His
ENST00000673971.1:c.*1798G>C ENSP00000501192.1:n.*1798G>C
ENST00000262795.5:c.3196G>C ENSP00000489147.1:p.Asp1066His
ENST00000414786.6:n.3384G>C
ENST00000445220.5:c.3178G>C ENSP00000489407.1:p.Asp1060His