Canonical Allele Identifier: CA515264916
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160683G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722255G>C , CM000684.2:g.50722255G>C GRCh38
NC_000022.10:g.51160683G>C , CM000684.1:g.51160683G>C GRCh37
NC_000022.9:g.49507549G>C NCBI36
NG_008607.2:g.52901G>C
NG_070230.1:g.58039G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4023G>C ENSP00000489147.2:p.Trp1341Cys
ENST00000414786.7:n.4607G>C
ENST00000445220.7:c.3075G>C ENSP00000489407.2:p.Trp1025Cys
ENST00000664402.2:c.2565G>C ENSP00000499475.1:p.Trp855Cys
ENST00000673971.2:c.*3021G>C ENSP00000501192.1:n.*3021G>C
ENST00000445220.6:c.3075G>C ENSP00000489407.2:p.Trp1025Cys
ENST00000262795.6:c.4023G>C ENSP00000489147.2:p.Trp1341Cys
ENST00000664402.1:c.2565G>C ENSP00000499475.1:p.Trp855Cys
ENST00000673971.1:c.*3021G>C ENSP00000501192.1:n.*3021G>C
ENST00000262795.5:c.4419G>C ENSP00000489147.1:p.Trp1473Cys
ENST00000414786.6:n.4607G>C
ENST00000445220.5:c.4401G>C ENSP00000489407.1:p.Trp1467Cys