Canonical Allele Identifier: CA515263731
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160291G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721863G>A , CM000684.2:g.50721863G>A GRCh38
NC_000022.10:g.51160291G>A , CM000684.1:g.51160291G>A GRCh37
NC_000022.9:g.49507157G>A NCBI36
NG_008607.2:g.52509G>A
NG_070230.1:g.57647G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3631G>A ENSP00000489147.2:p.Glu1211Lys
ENST00000414786.7:n.4215G>A
ENST00000445220.7:c.2683G>A ENSP00000489407.2:p.Glu895Lys
ENST00000664402.2:c.2173G>A ENSP00000499475.1:p.Glu725Lys
ENST00000673971.2:c.*2629G>A ENSP00000501192.1:n.*2629G>A
ENST00000445220.6:c.2683G>A ENSP00000489407.2:p.Glu895Lys
ENST00000262795.6:c.3631G>A ENSP00000489147.2:p.Glu1211Lys
ENST00000664402.1:c.2173G>A ENSP00000499475.1:p.Glu725Lys
ENST00000673971.1:c.*2629G>A ENSP00000501192.1:n.*2629G>A
ENST00000262795.5:c.4027G>A ENSP00000489147.1:p.Glu1343Lys
ENST00000414786.6:n.4215G>A
ENST00000445220.5:c.4009G>A ENSP00000489407.1:p.Glu1337Lys