Canonical Allele Identifier: CA515254880
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136005G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697577G>C , CM000684.2:g.50697577G>C GRCh38
NC_000022.10:g.51136005G>C , CM000684.1:g.51136005G>C GRCh37
NC_000022.9:g.49482871G>C NCBI36
NG_008607.2:g.28223G>C
NG_070230.1:g.33442G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.961G>C ENSP00000489147.2:p.Ala321Pro
ENST00000414786.7:n.1545G>C
ENST00000445220.7:c.13G>C ENSP00000489407.2:p.Ala5Pro
ENST00000673971.2:c.1318G>C ENSP00000501192.1:p.Ala440Pro
ENST00000445220.6:c.13G>C ENSP00000489407.2:p.Ala5Pro
ENST00000262795.6:c.961G>C ENSP00000489147.2:p.Ala321Pro
ENST00000673971.1:c.1318G>C ENSP00000501192.1:p.Ala440Pro
ENST00000673995.1:c.14G>C
ENST00000262795.5:c.1357G>C ENSP00000489147.1:p.Ala453Pro
ENST00000414786.6:n.1545G>C
ENST00000445220.5:c.1339G>C ENSP00000489407.1:p.Ala447Pro