Canonical Allele Identifier: CA515267313
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51169472C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50731044C>G , CM000684.2:g.50731044C>G GRCh38
NC_000022.10:g.51169472C>G , CM000684.1:g.51169472C>G GRCh37
NC_000022.9:g.49516338C>G NCBI36
NG_008607.2:g.61690C>G
NG_070230.1:g.66828C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4556C>G ENSP00000489147.2:p.Pro1519Arg
ENST00000414786.7:n.5140C>G
ENST00000445220.7:c.3608C>G ENSP00000489407.2:p.Pro1203Arg
ENST00000664402.2:c.3098C>G ENSP00000499475.1:p.Pro1033Arg
ENST00000673971.2:c.*3554C>G ENSP00000501192.1:n.*3554C>G
ENST00000445220.6:c.3608C>G ENSP00000489407.2:p.Pro1203Arg
ENST00000262795.6:c.4556C>G ENSP00000489147.2:p.Pro1519Arg
ENST00000659388.1:c.371C>G ENSP00000499632.1:p.Pro124Arg
ENST00000664402.1:c.3098C>G ENSP00000499475.1:p.Pro1033Arg
ENST00000673971.1:c.*3554C>G ENSP00000501192.1:n.*3554C>G
ENST00000262795.5:c.4925C>G ENSP00000489147.1:p.Pro1642Arg
ENST00000414786.6:n.5140C>G
ENST00000445220.5:c.4907C>G ENSP00000489407.1:p.Pro1636Arg