Canonical Allele Identifier: CA515264338
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160496T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722068T>G , CM000684.2:g.50722068T>G GRCh38
NC_000022.10:g.51160496T>G , CM000684.1:g.51160496T>G GRCh37
NC_000022.9:g.49507362T>G NCBI36
NG_008607.2:g.52714T>G
NG_070230.1:g.57852T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3836T>G ENSP00000489147.2:p.Val1279Gly
ENST00000414786.7:n.4420T>G
ENST00000445220.7:c.2888T>G ENSP00000489407.2:p.Val963Gly
ENST00000664402.2:c.2378T>G ENSP00000499475.1:p.Val793Gly
ENST00000673971.2:c.*2834T>G ENSP00000501192.1:n.*2834T>G
ENST00000445220.6:c.2888T>G ENSP00000489407.2:p.Val963Gly
ENST00000262795.6:c.3836T>G ENSP00000489147.2:p.Val1279Gly
ENST00000664402.1:c.2378T>G ENSP00000499475.1:p.Val793Gly
ENST00000673971.1:c.*2834T>G ENSP00000501192.1:n.*2834T>G
ENST00000262795.5:c.4232T>G ENSP00000489147.1:p.Val1411Gly
ENST00000414786.6:n.4420T>G
ENST00000445220.5:c.4214T>G ENSP00000489407.1:p.Val1405Gly