Canonical Allele Identifier: CA515260588
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs2146830369
MyVariant Identifiers: chr22:g.51159319C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720891C>G , CM000684.2:g.50720891C>G GRCh38
NC_000022.10:g.51159319C>G , CM000684.1:g.51159319C>G GRCh37
NC_000022.9:g.49506185C>G NCBI36
NG_008607.2:g.51537C>G
NG_070230.1:g.56675C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2659C>G ENSP00000489147.2:p.Leu887Val
ENST00000414786.7:n.3243C>G
ENST00000445220.7:c.1711C>G ENSP00000489407.2:p.Leu571Val
ENST00000664402.2:c.1201C>G ENSP00000499475.1:p.Leu401Val
ENST00000673971.2:c.*1657C>G ENSP00000501192.1:n.*1657C>G
ENST00000445220.6:c.1711C>G ENSP00000489407.2:p.Leu571Val
ENST00000262795.6:c.2659C>G ENSP00000489147.2:p.Leu887Val
ENST00000664402.1:c.1201C>G ENSP00000499475.1:p.Leu401Val
ENST00000673971.1:c.*1657C>G ENSP00000501192.1:n.*1657C>G
ENST00000262795.5:c.3055C>G ENSP00000489147.1:p.Leu1019Val
ENST00000414786.6:n.3243C>G
ENST00000445220.5:c.3037C>G ENSP00000489407.1:p.Leu1013Val