Canonical Allele Identifier: CA515264876
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160670G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722242G>T , CM000684.2:g.50722242G>T GRCh38
NC_000022.10:g.51160670G>T , CM000684.1:g.51160670G>T GRCh37
NC_000022.9:g.49507536G>T NCBI36
NG_008607.2:g.52888G>T
NG_070230.1:g.58026G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4010G>T ENSP00000489147.2:p.Arg1337Met
ENST00000414786.7:n.4594G>T
ENST00000445220.7:c.3062G>T ENSP00000489407.2:p.Arg1021Met
ENST00000664402.2:c.2552G>T ENSP00000499475.1:p.Arg851Met
ENST00000673971.2:c.*3008G>T ENSP00000501192.1:n.*3008G>T
ENST00000445220.6:c.3062G>T ENSP00000489407.2:p.Arg1021Met
ENST00000262795.6:c.4010G>T ENSP00000489147.2:p.Arg1337Met
ENST00000664402.1:c.2552G>T ENSP00000499475.1:p.Arg851Met
ENST00000673971.1:c.*3008G>T ENSP00000501192.1:n.*3008G>T
ENST00000262795.5:c.4406G>T ENSP00000489147.1:p.Arg1469Met
ENST00000414786.6:n.4594G>T
ENST00000445220.5:c.4388G>T ENSP00000489407.1:p.Arg1463Met