Canonical Allele Identifier: CA515262198

Gene: SHANK3

Linked Data

• dbSNP Id: rs1422257312
• gnomAD v3: 22-50721378-G-A
• gnomAD v4: 22-50721378-G-A
• MyVariant Identifiers: chr22:g.51159806G>A (hg19) ; chr22:g.50721378G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721378G>A , CM000684.2:g.50721378G>A	GRCh38
NC_000022.10:g.51159806G>A , CM000684.1:g.51159806G>A	GRCh37
NC_000022.9:g.49506672G>A	NCBI36
NG_008607.2:g.52024G>A
NG_070230.1:g.57162G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3146G>A	ENSP00000489147.2:p.Arg1049Gln
ENST00000414786.7:n.3730G>A
ENST00000445220.7:c.2198G>A	ENSP00000489407.2:p.Arg733Gln
ENST00000664402.2:c.1688G>A	ENSP00000499475.1:p.Arg563Gln
ENST00000673971.2:c.*2144G>A	ENSP00000501192.1:n.*2144G>A
ENST00000445220.6:c.2198G>A	ENSP00000489407.2:p.Arg733Gln
ENST00000262795.6:c.3146G>A	ENSP00000489147.2:p.Arg1049Gln
ENST00000664402.1:c.1688G>A	ENSP00000499475.1:p.Arg563Gln
ENST00000673971.1:c.*2144G>A	ENSP00000501192.1:n.*2144G>A
ENST00000262795.5:c.3542G>A	ENSP00000489147.1:p.Arg1181Gln
ENST00000414786.6:n.3730G>A
ENST00000445220.5:c.3524G>A	ENSP00000489407.1:p.Arg1175Gln