Canonical Allele Identifier: CA515260993

Gene: SHANK3

Linked Data

• dbSNP Id: rs1389876682
• gnomAD v2: 22-51159468-G-A
• gnomAD v4: 22-50721040-G-A
• MyVariant Identifiers: chr22:g.51159468G>A (hg19) ; chr22:g.50721040G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721040G>A , CM000684.2:g.50721040G>A	GRCh38
NC_000022.10:g.51159468G>A , CM000684.1:g.51159468G>A	GRCh37
NC_000022.9:g.49506334G>A	NCBI36
NG_008607.2:g.51686G>A
NG_070230.1:g.56824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.2808G>A	ENSP00000489147.2:p.Leu936=
ENST00000414786.7:n.3392G>A
ENST00000445220.7:c.1860G>A	ENSP00000489407.2:p.Leu620=
ENST00000664402.2:c.1350G>A	ENSP00000499475.1:p.Leu450=
ENST00000673971.2:c.*1806G>A	ENSP00000501192.1:n.*1806G>A
ENST00000445220.6:c.1860G>A	ENSP00000489407.2:p.Leu620=
ENST00000262795.6:c.2808G>A	ENSP00000489147.2:p.Leu936=
ENST00000664402.1:c.1350G>A	ENSP00000499475.1:p.Leu450=
ENST00000673971.1:c.*1806G>A	ENSP00000501192.1:n.*1806G>A
ENST00000262795.5:c.3204G>A	ENSP00000489147.1:p.Leu1068=
ENST00000414786.6:n.3392G>A
ENST00000445220.5:c.3186G>A	ENSP00000489407.1:p.Leu1062=