Canonical Allele Identifier: CA515262832
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159980C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721552C>G , CM000684.2:g.50721552C>G GRCh38
NC_000022.10:g.51159980C>G , CM000684.1:g.51159980C>G GRCh37
NC_000022.9:g.49506846C>G NCBI36
NG_008607.2:g.52198C>G
NG_070230.1:g.57336C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3320C>G ENSP00000489147.2:p.Ala1107Gly
ENST00000414786.7:n.3904C>G
ENST00000445220.7:c.2372C>G ENSP00000489407.2:p.Ala791Gly
ENST00000664402.2:c.1862C>G ENSP00000499475.1:p.Ala621Gly
ENST00000673971.2:c.*2318C>G ENSP00000501192.1:n.*2318C>G
ENST00000445220.6:c.2372C>G ENSP00000489407.2:p.Ala791Gly
ENST00000262795.6:c.3320C>G ENSP00000489147.2:p.Ala1107Gly
ENST00000664402.1:c.1862C>G ENSP00000499475.1:p.Ala621Gly
ENST00000673971.1:c.*2318C>G ENSP00000501192.1:n.*2318C>G
ENST00000262795.5:c.3716C>G ENSP00000489147.1:p.Ala1239Gly
ENST00000414786.6:n.3904C>G
ENST00000445220.5:c.3698C>G ENSP00000489407.1:p.Ala1233Gly