Canonical Allele Identifier: CA515263917
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160347A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721919A>C , CM000684.2:g.50721919A>C GRCh38
NC_000022.10:g.51160347A>C , CM000684.1:g.51160347A>C GRCh37
NC_000022.9:g.49507213A>C NCBI36
NG_008607.2:g.52565A>C
NG_070230.1:g.57703A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3687A>C ENSP00000489147.2:p.Thr1229=
ENST00000414786.7:n.4271A>C
ENST00000445220.7:c.2739A>C ENSP00000489407.2:p.Thr913=
ENST00000664402.2:c.2229A>C ENSP00000499475.1:p.Thr743=
ENST00000673971.2:c.*2685A>C ENSP00000501192.1:n.*2685A>C
ENST00000445220.6:c.2739A>C ENSP00000489407.2:p.Thr913=
ENST00000262795.6:c.3687A>C ENSP00000489147.2:p.Thr1229=
ENST00000664402.1:c.2229A>C ENSP00000499475.1:p.Thr743=
ENST00000673971.1:c.*2685A>C ENSP00000501192.1:n.*2685A>C
ENST00000262795.5:c.4083A>C ENSP00000489147.1:p.Thr1361=
ENST00000414786.6:n.4271A>C
ENST00000445220.5:c.4065A>C ENSP00000489407.1:p.Thr1355=