Canonical Allele Identifier: CA10326068

Gene: SHANK3

Linked Data

• ClinVar Variation Id: 588727
• ClinVar RCV Id: RCV002313664
• dbSNP Id: rs752694316
• ExAC: 22:51159815 G / A
• gnomAD v2: 22-51159815-G-A
• gnomAD v3: 22-50721387-G-A
• gnomAD v4: 22-50721387-G-A
• MyVariant Identifiers: chr22:g.51159815G>A (hg19) ; chr22:g.50721387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721387G>A , CM000684.2:g.50721387G>A	GRCh38
NC_000022.10:g.51159815G>A , CM000684.1:g.51159815G>A	GRCh37
NC_000022.9:g.49506681G>A	NCBI36
NG_008607.2:g.52033G>A
NG_070230.1:g.57171G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3155G>A	ENSP00000489147.2:p.Arg1052Gln
ENST00000414786.7:n.3739G>A
ENST00000445220.7:c.2207G>A	ENSP00000489407.2:p.Arg736Gln
ENST00000664402.2:c.1697G>A	ENSP00000499475.1:p.Arg566Gln
ENST00000673971.2:c.*2153G>A	ENSP00000501192.1:n.*2153G>A
ENST00000445220.6:c.2207G>A	ENSP00000489407.2:p.Arg736Gln
ENST00000262795.6:c.3155G>A	ENSP00000489147.2:p.Arg1052Gln
ENST00000664402.1:c.1697G>A	ENSP00000499475.1:p.Arg566Gln
ENST00000673971.1:c.*2153G>A	ENSP00000501192.1:n.*2153G>A
ENST00000262795.5:c.3551G>A	ENSP00000489147.1:p.Arg1184Gln
ENST00000414786.6:n.3739G>A
ENST00000445220.5:c.3533G>A	ENSP00000489407.1:p.Arg1178Gln