Canonical Allele Identifier: CA515262452
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159877C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721449C>A , CM000684.2:g.50721449C>A GRCh38
NC_000022.10:g.51159877C>A , CM000684.1:g.51159877C>A GRCh37
NC_000022.9:g.49506743C>A NCBI36
NG_008607.2:g.52095C>A
NG_070230.1:g.57233C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3217C>A ENSP00000489147.2:p.Pro1073Thr
ENST00000414786.7:n.3801C>A
ENST00000445220.7:c.2269C>A ENSP00000489407.2:p.Pro757Thr
ENST00000664402.2:c.1759C>A ENSP00000499475.1:p.Pro587Thr
ENST00000673971.2:c.*2215C>A ENSP00000501192.1:n.*2215C>A
ENST00000445220.6:c.2269C>A ENSP00000489407.2:p.Pro757Thr
ENST00000262795.6:c.3217C>A ENSP00000489147.2:p.Pro1073Thr
ENST00000664402.1:c.1759C>A ENSP00000499475.1:p.Pro587Thr
ENST00000673971.1:c.*2215C>A ENSP00000501192.1:n.*2215C>A
ENST00000262795.5:c.3613C>A ENSP00000489147.1:p.Pro1205Thr
ENST00000414786.6:n.3801C>A
ENST00000445220.5:c.3595C>A ENSP00000489407.1:p.Pro1199Thr