Canonical Allele Identifier: CA515260489
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159284C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720856C>G , CM000684.2:g.50720856C>G GRCh38
NC_000022.10:g.51159284C>G , CM000684.1:g.51159284C>G GRCh37
NC_000022.9:g.49506150C>G NCBI36
NG_008607.2:g.51502C>G
NG_070230.1:g.56640C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2624C>G ENSP00000489147.2:p.Ala875Gly
ENST00000414786.7:n.3208C>G
ENST00000445220.7:c.1676C>G ENSP00000489407.2:p.Ala559Gly
ENST00000664402.2:c.1166C>G ENSP00000499475.1:p.Ala389Gly
ENST00000673971.2:c.*1622C>G ENSP00000501192.1:n.*1622C>G
ENST00000445220.6:c.1676C>G ENSP00000489407.2:p.Ala559Gly
ENST00000262795.6:c.2624C>G ENSP00000489147.2:p.Ala875Gly
ENST00000664402.1:c.1166C>G ENSP00000499475.1:p.Ala389Gly
ENST00000673971.1:c.*1622C>G ENSP00000501192.1:n.*1622C>G
ENST00000262795.5:c.3020C>G ENSP00000489147.1:p.Ala1007Gly
ENST00000414786.6:n.3208C>G
ENST00000445220.5:c.3002C>G ENSP00000489407.1:p.Ala1001Gly