Canonical Allele Identifier: CA515258802
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51158711C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720283C>G , CM000684.2:g.50720283C>G GRCh38
NC_000022.10:g.51158711C>G , CM000684.1:g.51158711C>G GRCh37
NC_000022.9:g.49505577C>G NCBI36
NG_008607.2:g.50929C>G
NG_070230.1:g.56067C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2051C>G ENSP00000489147.2:p.Pro684Arg
ENST00000414786.7:n.2635C>G
ENST00000445220.7:c.1103C>G ENSP00000489407.2:p.Pro368Arg
ENST00000664402.2:c.593C>G ENSP00000499475.1:p.Pro198Arg
ENST00000673971.2:c.*1049C>G ENSP00000501192.1:n.*1049C>G
ENST00000445220.6:c.1103C>G ENSP00000489407.2:p.Pro368Arg
ENST00000262795.6:c.2051C>G ENSP00000489147.2:p.Pro684Arg
ENST00000664402.1:c.593C>G ENSP00000499475.1:p.Pro198Arg
ENST00000673971.1:c.*1049C>G ENSP00000501192.1:n.*1049C>G
ENST00000262795.5:c.2447C>G ENSP00000489147.1:p.Pro816Arg
ENST00000414786.6:n.2635C>G
ENST00000445220.5:c.2429C>G ENSP00000489407.1:p.Pro810Arg