Canonical Allele Identifier: CA515254969
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs2083091146
MyVariant Identifiers: chr22:g.51136036A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697608A>C , CM000684.2:g.50697608A>C GRCh38
NC_000022.10:g.51136036A>C , CM000684.1:g.51136036A>C GRCh37
NC_000022.9:g.49482902A>C NCBI36
NG_008607.2:g.28254A>C
NG_070230.1:g.33473A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.992A>C ENSP00000489147.2:p.Lys331Thr
ENST00000414786.7:n.1576A>C
ENST00000445220.7:c.44A>C ENSP00000489407.2:p.Lys15Thr
ENST00000673971.2:c.1349A>C ENSP00000501192.1:p.Lys450Thr
ENST00000445220.6:c.44A>C ENSP00000489407.2:p.Lys15Thr
ENST00000262795.6:c.992A>C ENSP00000489147.2:p.Lys331Thr
ENST00000673971.1:c.1349A>C ENSP00000501192.1:p.Lys450Thr
ENST00000673995.1:c.45A>C
ENST00000262795.5:c.1388A>C ENSP00000489147.1:p.Lys463Thr
ENST00000414786.6:n.1576A>C
ENST00000445220.5:c.1370A>C ENSP00000489407.1:p.Lys457Thr