Canonical Allele Identifier: CA515261763

Gene: SHANK3

Linked Data

• dbSNP Id: rs1278449166
• gnomAD v2: 22-51159737-C-A
• gnomAD v3: 22-50721309-C-A
• gnomAD v4: 22-50721309-C-A
• MyVariant Identifiers: chr22:g.51159737C>A (hg19) ; chr22:g.50721309C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721309C>A , CM000684.2:g.50721309C>A	GRCh38
NC_000022.10:g.51159737C>A , CM000684.1:g.51159737C>A	GRCh37
NC_000022.9:g.49506603C>A	NCBI36
NG_008607.2:g.51955C>A
NG_070230.1:g.57093C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3077C>A	ENSP00000489147.2:p.Pro1026Gln
ENST00000414786.7:n.3661C>A
ENST00000445220.7:c.2129C>A	ENSP00000489407.2:p.Pro710Gln
ENST00000664402.2:c.1619C>A	ENSP00000499475.1:p.Pro540Gln
ENST00000673971.2:c.*2075C>A	ENSP00000501192.1:n.*2075C>A
ENST00000445220.6:c.2129C>A	ENSP00000489407.2:p.Pro710Gln
ENST00000262795.6:c.3077C>A	ENSP00000489147.2:p.Pro1026Gln
ENST00000664402.1:c.1619C>A	ENSP00000499475.1:p.Pro540Gln
ENST00000673971.1:c.*2075C>A	ENSP00000501192.1:n.*2075C>A
ENST00000262795.5:c.3473C>A	ENSP00000489147.1:p.Pro1158Gln
ENST00000414786.6:n.3661C>A
ENST00000445220.5:c.3455C>A	ENSP00000489407.1:p.Pro1152Gln