Canonical Allele Identifier: CA515255088
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136078C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697650C>A , CM000684.2:g.50697650C>A GRCh38
NC_000022.10:g.51136078C>A , CM000684.1:g.51136078C>A GRCh37
NC_000022.9:g.49482944C>A NCBI36
NG_008607.2:g.28296C>A
NG_070230.1:g.33515C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.1034C>A ENSP00000489147.2:p.Ala345Asp
ENST00000414786.7:n.1618C>A
ENST00000445220.7:c.86C>A ENSP00000489407.2:p.Ala29Asp
ENST00000673971.2:c.1391C>A ENSP00000501192.1:p.Ala464Asp
ENST00000445220.6:c.86C>A ENSP00000489407.2:p.Ala29Asp
ENST00000262795.6:c.1034C>A ENSP00000489147.2:p.Ala345Asp
ENST00000673971.1:c.1391C>A ENSP00000501192.1:p.Ala464Asp
ENST00000673995.1:c.87C>A
ENST00000262795.5:c.1430C>A ENSP00000489147.1:p.Ala477Asp
ENST00000414786.6:n.1618C>A
ENST00000445220.5:c.1412C>A ENSP00000489407.1:p.Ala471Asp