Canonical Allele Identifier: CA515259928

Gene: SHANK3

Linked Data

• dbSNP Id: rs1435109768
• gnomAD v2: 22-51159089-C-T
• gnomAD v3: 22-50720661-C-T
• gnomAD v4: 22-50720661-C-T
• MyVariant Identifiers: chr22:g.51159089C>T (hg19) ; chr22:g.50720661C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50720661C>T , CM000684.2:g.50720661C>T	GRCh38
NC_000022.10:g.51159089C>T , CM000684.1:g.51159089C>T	GRCh37
NC_000022.9:g.49505955C>T	NCBI36
NG_008607.2:g.51307C>T
NG_070230.1:g.56445C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.2429C>T	ENSP00000489147.2:p.Ala810Val
ENST00000414786.7:n.3013C>T
ENST00000445220.7:c.1481C>T	ENSP00000489407.2:p.Ala494Val
ENST00000664402.2:c.971C>T	ENSP00000499475.1:p.Ala324Val
ENST00000673971.2:c.*1427C>T	ENSP00000501192.1:n.*1427C>T
ENST00000445220.6:c.1481C>T	ENSP00000489407.2:p.Ala494Val
ENST00000262795.6:c.2429C>T	ENSP00000489147.2:p.Ala810Val
ENST00000664402.1:c.971C>T	ENSP00000499475.1:p.Ala324Val
ENST00000673971.1:c.*1427C>T	ENSP00000501192.1:n.*1427C>T
ENST00000262795.5:c.2825C>T	ENSP00000489147.1:p.Ala942Val
ENST00000414786.6:n.3013C>T
ENST00000445220.5:c.2807C>T	ENSP00000489407.1:p.Ala936Val