Canonical Allele Identifier: CA515264372
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160507C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722079C>A , CM000684.2:g.50722079C>A GRCh38
NC_000022.10:g.51160507C>A , CM000684.1:g.51160507C>A GRCh37
NC_000022.9:g.49507373C>A NCBI36
NG_008607.2:g.52725C>A
NG_070230.1:g.57863C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3847C>A ENSP00000489147.2:p.Pro1283Thr
ENST00000414786.7:n.4431C>A
ENST00000445220.7:c.2899C>A ENSP00000489407.2:p.Pro967Thr
ENST00000664402.2:c.2389C>A ENSP00000499475.1:p.Pro797Thr
ENST00000673971.2:c.*2845C>A ENSP00000501192.1:n.*2845C>A
ENST00000445220.6:c.2899C>A ENSP00000489407.2:p.Pro967Thr
ENST00000262795.6:c.3847C>A ENSP00000489147.2:p.Pro1283Thr
ENST00000664402.1:c.2389C>A ENSP00000499475.1:p.Pro797Thr
ENST00000673971.1:c.*2845C>A ENSP00000501192.1:n.*2845C>A
ENST00000262795.5:c.4243C>A ENSP00000489147.1:p.Pro1415Thr
ENST00000414786.6:n.4431C>A
ENST00000445220.5:c.4225C>A ENSP00000489407.1:p.Pro1409Thr