Canonical Allele Identifier: CA515264871
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160669A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722241A>G , CM000684.2:g.50722241A>G GRCh38
NC_000022.10:g.51160669A>G , CM000684.1:g.51160669A>G GRCh37
NC_000022.9:g.49507535A>G NCBI36
NG_008607.2:g.52887A>G
NG_070230.1:g.58025A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4009A>G ENSP00000489147.2:p.Arg1337Gly
ENST00000414786.7:n.4593A>G
ENST00000445220.7:c.3061A>G ENSP00000489407.2:p.Arg1021Gly
ENST00000664402.2:c.2551A>G ENSP00000499475.1:p.Arg851Gly
ENST00000673971.2:c.*3007A>G ENSP00000501192.1:n.*3007A>G
ENST00000445220.6:c.3061A>G ENSP00000489407.2:p.Arg1021Gly
ENST00000262795.6:c.4009A>G ENSP00000489147.2:p.Arg1337Gly
ENST00000664402.1:c.2551A>G ENSP00000499475.1:p.Arg851Gly
ENST00000673971.1:c.*3007A>G ENSP00000501192.1:n.*3007A>G
ENST00000262795.5:c.4405A>G ENSP00000489147.1:p.Arg1469Gly
ENST00000414786.6:n.4593A>G
ENST00000445220.5:c.4387A>G ENSP00000489407.1:p.Arg1463Gly