Canonical Allele Identifier: CA10326240

Gene: SHANK3

Linked Data

• ClinVar Variation Id: 1697109
• ClinVar RCV Id: RCV002267455
• dbSNP Id: rs752413653
• ExAC: 22:51160556 C / T
• gnomAD v2: 22-51160556-C-T
• gnomAD v3: 22-50722128-C-T
• gnomAD v4: 22-50722128-C-T
• COSMIC: COSM4105266 ; COSM4105267
• MyVariant Identifiers: chr22:g.51160556C>T (hg19) ; chr22:g.50722128C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50722128C>T , CM000684.2:g.50722128C>T	GRCh38
NC_000022.10:g.51160556C>T , CM000684.1:g.51160556C>T	GRCh37
NC_000022.9:g.49507422C>T	NCBI36
NG_008607.2:g.52774C>T
NG_070230.1:g.57912C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3896C>T	ENSP00000489147.2:p.Pro1299Leu
ENST00000414786.7:n.4480C>T
ENST00000445220.7:c.2948C>T	ENSP00000489407.2:p.Pro983Leu
ENST00000664402.2:c.2438C>T	ENSP00000499475.1:p.Pro813Leu
ENST00000673971.2:c.*2894C>T	ENSP00000501192.1:n.*2894C>T
ENST00000445220.6:c.2948C>T	ENSP00000489407.2:p.Pro983Leu
ENST00000262795.6:c.3896C>T	ENSP00000489147.2:p.Pro1299Leu
ENST00000664402.1:c.2438C>T	ENSP00000499475.1:p.Pro813Leu
ENST00000673971.1:c.*2894C>T	ENSP00000501192.1:n.*2894C>T
ENST00000262795.5:c.4292C>T	ENSP00000489147.1:p.Pro1431Leu
ENST00000414786.6:n.4480C>T
ENST00000445220.5:c.4274C>T	ENSP00000489407.1:p.Pro1425Leu