Canonical Allele Identifier: CA515254882
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136006C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697578C>G , CM000684.2:g.50697578C>G GRCh38
NC_000022.10:g.51136006C>G , CM000684.1:g.51136006C>G GRCh37
NC_000022.9:g.49482872C>G NCBI36
NG_008607.2:g.28224C>G
NG_070230.1:g.33443C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.962C>G ENSP00000489147.2:p.Ala321Gly
ENST00000414786.7:n.1546C>G
ENST00000445220.7:c.14C>G ENSP00000489407.2:p.Ala5Gly
ENST00000673971.2:c.1319C>G ENSP00000501192.1:p.Ala440Gly
ENST00000445220.6:c.14C>G ENSP00000489407.2:p.Ala5Gly
ENST00000262795.6:c.962C>G ENSP00000489147.2:p.Ala321Gly
ENST00000673971.1:c.1319C>G ENSP00000501192.1:p.Ala440Gly
ENST00000673995.1:c.15C>G
ENST00000262795.5:c.1358C>G ENSP00000489147.1:p.Ala453Gly
ENST00000414786.6:n.1546C>G
ENST00000445220.5:c.1340C>G ENSP00000489407.1:p.Ala447Gly