Canonical Allele Identifier: CA515262965

Gene: SHANK3

Linked Data

• dbSNP Id: rs773082364
• gnomAD v2: 22-51160024-C-G
• gnomAD v3: 22-50721596-C-G
• gnomAD v4: 22-50721596-C-G
• MyVariant Identifiers: chr22:g.51160024C>G (hg19) ; chr22:g.50721596C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721596C>G , CM000684.2:g.50721596C>G	GRCh38
NC_000022.10:g.51160024C>G , CM000684.1:g.51160024C>G	GRCh37
NC_000022.9:g.49506890C>G	NCBI36
NG_008607.2:g.52242C>G
NG_070230.1:g.57380C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3364C>G	ENSP00000489147.2:p.Arg1122Gly
ENST00000414786.7:n.3948C>G
ENST00000445220.7:c.2416C>G	ENSP00000489407.2:p.Arg806Gly
ENST00000664402.2:c.1906C>G	ENSP00000499475.1:p.Arg636Gly
ENST00000673971.2:c.*2362C>G	ENSP00000501192.1:n.*2362C>G
ENST00000445220.6:c.2416C>G	ENSP00000489407.2:p.Arg806Gly
ENST00000262795.6:c.3364C>G	ENSP00000489147.2:p.Arg1122Gly
ENST00000664402.1:c.1906C>G	ENSP00000499475.1:p.Arg636Gly
ENST00000673971.1:c.*2362C>G	ENSP00000501192.1:n.*2362C>G
ENST00000262795.5:c.3760C>G	ENSP00000489147.1:p.Arg1254Gly
ENST00000414786.6:n.3948C>G
ENST00000445220.5:c.3742C>G	ENSP00000489407.1:p.Arg1248Gly