Canonical Allele Identifier: CA515254951
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136030G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697602G>A , CM000684.2:g.50697602G>A GRCh38
NC_000022.10:g.51136030G>A , CM000684.1:g.51136030G>A GRCh37
NC_000022.9:g.49482896G>A NCBI36
NG_008607.2:g.28248G>A
NG_070230.1:g.33467G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.986G>A ENSP00000489147.2:p.Gly329Asp
ENST00000414786.7:n.1570G>A
ENST00000445220.7:c.38G>A ENSP00000489407.2:p.Gly13Asp
ENST00000673971.2:c.1343G>A ENSP00000501192.1:p.Gly448Asp
ENST00000445220.6:c.38G>A ENSP00000489407.2:p.Gly13Asp
ENST00000262795.6:c.986G>A ENSP00000489147.2:p.Gly329Asp
ENST00000673971.1:c.1343G>A ENSP00000501192.1:p.Gly448Asp
ENST00000673995.1:c.39G>A
ENST00000262795.5:c.1382G>A ENSP00000489147.1:p.Gly461Asp
ENST00000414786.6:n.1570G>A
ENST00000445220.5:c.1364G>A ENSP00000489407.1:p.Gly455Asp