Canonical Allele Identifier: CA515262128
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159785G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721357G>C , CM000684.2:g.50721357G>C GRCh38
NC_000022.10:g.51159785G>C , CM000684.1:g.51159785G>C GRCh37
NC_000022.9:g.49506651G>C NCBI36
NG_008607.2:g.52003G>C
NG_070230.1:g.57141G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3125G>C ENSP00000489147.2:p.Arg1042Thr
ENST00000414786.7:n.3709G>C
ENST00000445220.7:c.2177G>C ENSP00000489407.2:p.Arg726Thr
ENST00000664402.2:c.1667G>C ENSP00000499475.1:p.Arg556Thr
ENST00000673971.2:c.*2123G>C ENSP00000501192.1:n.*2123G>C
ENST00000445220.6:c.2177G>C ENSP00000489407.2:p.Arg726Thr
ENST00000262795.6:c.3125G>C ENSP00000489147.2:p.Arg1042Thr
ENST00000664402.1:c.1667G>C ENSP00000499475.1:p.Arg556Thr
ENST00000673971.1:c.*2123G>C ENSP00000501192.1:n.*2123G>C
ENST00000262795.5:c.3521G>C ENSP00000489147.1:p.Arg1174Thr
ENST00000414786.6:n.3709G>C
ENST00000445220.5:c.3503G>C ENSP00000489407.1:p.Arg1168Thr