Canonical Allele Identifier: CA10326083

Gene: SHANK3

Linked Data

• dbSNP Id: rs763211639
• ExAC: 22:51159877 C / T
• gnomAD v2: 22-51159877-C-T
• gnomAD v3: 22-50721449-C-T
• gnomAD v4: 22-50721449-C-T
• MyVariant Identifiers: chr22:g.51159877C>T (hg19) ; chr22:g.50721449C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721449C>T , CM000684.2:g.50721449C>T	GRCh38
NC_000022.10:g.51159877C>T , CM000684.1:g.51159877C>T	GRCh37
NC_000022.9:g.49506743C>T	NCBI36
NG_008607.2:g.52095C>T
NG_070230.1:g.57233C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3217C>T	ENSP00000489147.2:p.Pro1073Ser
ENST00000414786.7:n.3801C>T
ENST00000445220.7:c.2269C>T	ENSP00000489407.2:p.Pro757Ser
ENST00000664402.2:c.1759C>T	ENSP00000499475.1:p.Pro587Ser
ENST00000673971.2:c.*2215C>T	ENSP00000501192.1:n.*2215C>T
ENST00000445220.6:c.2269C>T	ENSP00000489407.2:p.Pro757Ser
ENST00000262795.6:c.3217C>T	ENSP00000489147.2:p.Pro1073Ser
ENST00000664402.1:c.1759C>T	ENSP00000499475.1:p.Pro587Ser
ENST00000673971.1:c.*2215C>T	ENSP00000501192.1:n.*2215C>T
ENST00000262795.5:c.3613C>T	ENSP00000489147.1:p.Pro1205Ser
ENST00000414786.6:n.3801C>T
ENST00000445220.5:c.3595C>T	ENSP00000489407.1:p.Pro1199Ser