Canonical Allele Identifier: CA515263599

Gene: SHANK3

Linked Data

• dbSNP Id: rs1378832448
• gnomAD v2: 22-51160249-C-G
• MyVariant Identifiers: chr22:g.51160249C>G (hg19) ; chr22:g.50721821C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721821C>G , CM000684.2:g.50721821C>G	GRCh38
NC_000022.10:g.51160249C>G , CM000684.1:g.51160249C>G	GRCh37
NC_000022.9:g.49507115C>G	NCBI36
NG_008607.2:g.52467C>G
NG_070230.1:g.57605C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3589C>G	ENSP00000489147.2:p.Pro1197Ala
ENST00000414786.7:n.4173C>G
ENST00000445220.7:c.2641C>G	ENSP00000489407.2:p.Pro881Ala
ENST00000664402.2:c.2131C>G	ENSP00000499475.1:p.Pro711Ala
ENST00000673971.2:c.*2587C>G	ENSP00000501192.1:n.*2587C>G
ENST00000445220.6:c.2641C>G	ENSP00000489407.2:p.Pro881Ala
ENST00000262795.6:c.3589C>G	ENSP00000489147.2:p.Pro1197Ala
ENST00000664402.1:c.2131C>G	ENSP00000499475.1:p.Pro711Ala
ENST00000673971.1:c.*2587C>G	ENSP00000501192.1:n.*2587C>G
ENST00000262795.5:c.3985C>G	ENSP00000489147.1:p.Pro1329Ala
ENST00000414786.6:n.4173C>G
ENST00000445220.5:c.3967C>G	ENSP00000489407.1:p.Pro1323Ala