Canonical Allele Identifier: CA515262131

Gene: SHANK3

Linked Data

• dbSNP Id: rs1255395251
• gnomAD v2: 22-51159786-G-A
• gnomAD v3: 22-50721358-G-A
• gnomAD v4: 22-50721358-G-A
• MyVariant Identifiers: chr22:g.51159786G>A (hg19) ; chr22:g.50721358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721358G>A , CM000684.2:g.50721358G>A	GRCh38
NC_000022.10:g.51159786G>A , CM000684.1:g.51159786G>A	GRCh37
NC_000022.9:g.49506652G>A	NCBI36
NG_008607.2:g.52004G>A
NG_070230.1:g.57142G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3126G>A	ENSP00000489147.2:p.Arg1042=
ENST00000414786.7:n.3710G>A
ENST00000445220.7:c.2178G>A	ENSP00000489407.2:p.Arg726=
ENST00000664402.2:c.1668G>A	ENSP00000499475.1:p.Arg556=
ENST00000673971.2:c.*2124G>A	ENSP00000501192.1:n.*2124G>A
ENST00000445220.6:c.2178G>A	ENSP00000489407.2:p.Arg726=
ENST00000262795.6:c.3126G>A	ENSP00000489147.2:p.Arg1042=
ENST00000664402.1:c.1668G>A	ENSP00000499475.1:p.Arg556=
ENST00000673971.1:c.*2124G>A	ENSP00000501192.1:n.*2124G>A
ENST00000262795.5:c.3522G>A	ENSP00000489147.1:p.Arg1174=
ENST00000414786.6:n.3710G>A
ENST00000445220.5:c.3504G>A	ENSP00000489407.1:p.Arg1168=