Canonical Allele Identifier: CA515267333

Gene: SHANK3

Linked Data

• MyVariant Identifiers: chr22:g.51169477C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50731049C>A , CM000684.2:g.50731049C>A	GRCh38
NC_000022.10:g.51169477C>A , CM000684.1:g.51169477C>A	GRCh37
NC_000022.9:g.49516343C>A	NCBI36
NG_008607.2:g.61695C>A
NG_070230.1:g.66833C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.4561C>A	ENSP00000489147.2:p.Pro1521Thr
ENST00000414786.7:n.5145C>A
ENST00000445220.7:c.3613C>A	ENSP00000489407.2:p.Pro1205Thr
ENST00000664402.2:c.3103C>A	ENSP00000499475.1:p.Pro1035Thr
ENST00000673971.2:c.*3559C>A	ENSP00000501192.1:n.*3559C>A
ENST00000445220.6:c.3613C>A	ENSP00000489407.2:p.Pro1205Thr
ENST00000262795.6:c.4561C>A	ENSP00000489147.2:p.Pro1521Thr
ENST00000659388.1:c.376C>A	ENSP00000499632.1:p.Pro126Thr
ENST00000664402.1:c.3103C>A	ENSP00000499475.1:p.Pro1035Thr
ENST00000673971.1:c.*3559C>A	ENSP00000501192.1:n.*3559C>A
ENST00000262795.5:c.4930C>A	ENSP00000489147.1:p.Pro1644Thr
ENST00000414786.6:n.5145C>A
ENST00000445220.5:c.4912C>A	ENSP00000489407.1:p.Pro1638Thr