Canonical Allele Identifier: CA515260286
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159214C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720786C>G , CM000684.2:g.50720786C>G GRCh38
NC_000022.10:g.51159214C>G , CM000684.1:g.51159214C>G GRCh37
NC_000022.9:g.49506080C>G NCBI36
NG_008607.2:g.51432C>G
NG_070230.1:g.56570C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2554C>G ENSP00000489147.2:p.Pro852Ala
ENST00000414786.7:n.3138C>G
ENST00000445220.7:c.1606C>G ENSP00000489407.2:p.Pro536Ala
ENST00000664402.2:c.1096C>G ENSP00000499475.1:p.Pro366Ala
ENST00000673971.2:c.*1552C>G ENSP00000501192.1:n.*1552C>G
ENST00000445220.6:c.1606C>G ENSP00000489407.2:p.Pro536Ala
ENST00000262795.6:c.2554C>G ENSP00000489147.2:p.Pro852Ala
ENST00000664402.1:c.1096C>G ENSP00000499475.1:p.Pro366Ala
ENST00000673971.1:c.*1552C>G ENSP00000501192.1:n.*1552C>G
ENST00000262795.5:c.2950C>G ENSP00000489147.1:p.Pro984Ala
ENST00000414786.6:n.3138C>G
ENST00000445220.5:c.2932C>G ENSP00000489407.1:p.Pro978Ala