Canonical Allele Identifier: CA515262703

Gene: SHANK3

Linked Data

• dbSNP Id: rs1210992538
• gnomAD v2: 22-51159941-C-G
• gnomAD v3: 22-50721513-C-G
• gnomAD v4: 22-50721513-C-G
• MyVariant Identifiers: chr22:g.51159941C>G (hg19) ; chr22:g.50721513C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721513C>G , CM000684.2:g.50721513C>G	GRCh38
NC_000022.10:g.51159941C>G , CM000684.1:g.51159941C>G	GRCh37
NC_000022.9:g.49506807C>G	NCBI36
NG_008607.2:g.52159C>G
NG_070230.1:g.57297C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3281C>G	ENSP00000489147.2:p.Ala1094Gly
ENST00000414786.7:n.3865C>G
ENST00000445220.7:c.2333C>G	ENSP00000489407.2:p.Ala778Gly
ENST00000664402.2:c.1823C>G	ENSP00000499475.1:p.Ala608Gly
ENST00000673971.2:c.*2279C>G	ENSP00000501192.1:n.*2279C>G
ENST00000445220.6:c.2333C>G	ENSP00000489407.2:p.Ala778Gly
ENST00000262795.6:c.3281C>G	ENSP00000489147.2:p.Ala1094Gly
ENST00000664402.1:c.1823C>G	ENSP00000499475.1:p.Ala608Gly
ENST00000673971.1:c.*2279C>G	ENSP00000501192.1:n.*2279C>G
ENST00000262795.5:c.3677C>G	ENSP00000489147.1:p.Ala1226Gly
ENST00000414786.6:n.3865C>G
ENST00000445220.5:c.3659C>G	ENSP00000489407.1:p.Ala1220Gly