Canonical Allele Identifier: CA515262271
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159828G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721400G>C , CM000684.2:g.50721400G>C GRCh38
NC_000022.10:g.51159828G>C , CM000684.1:g.51159828G>C GRCh37
NC_000022.9:g.49506694G>C NCBI36
NG_008607.2:g.52046G>C
NG_070230.1:g.57184G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3168G>C ENSP00000489147.2:p.Glu1056Asp
ENST00000414786.7:n.3752G>C
ENST00000445220.7:c.2220G>C ENSP00000489407.2:p.Glu740Asp
ENST00000664402.2:c.1710G>C ENSP00000499475.1:p.Glu570Asp
ENST00000673971.2:c.*2166G>C ENSP00000501192.1:n.*2166G>C
ENST00000445220.6:c.2220G>C ENSP00000489407.2:p.Glu740Asp
ENST00000262795.6:c.3168G>C ENSP00000489147.2:p.Glu1056Asp
ENST00000664402.1:c.1710G>C ENSP00000499475.1:p.Glu570Asp
ENST00000673971.1:c.*2166G>C ENSP00000501192.1:n.*2166G>C
ENST00000262795.5:c.3564G>C ENSP00000489147.1:p.Glu1188Asp
ENST00000414786.6:n.3752G>C
ENST00000445220.5:c.3546G>C ENSP00000489407.1:p.Glu1182Asp