Canonical Allele Identifier: CA515260010
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159117C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720689C>A , CM000684.2:g.50720689C>A GRCh38
NC_000022.10:g.51159117C>A , CM000684.1:g.51159117C>A GRCh37
NC_000022.9:g.49505983C>A NCBI36
NG_008607.2:g.51335C>A
NG_070230.1:g.56473C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2457C>A ENSP00000489147.2:p.Ser819Arg
ENST00000414786.7:n.3041C>A
ENST00000445220.7:c.1509C>A ENSP00000489407.2:p.Ser503Arg
ENST00000664402.2:c.999C>A ENSP00000499475.1:p.Ser333Arg
ENST00000673971.2:c.*1455C>A ENSP00000501192.1:n.*1455C>A
ENST00000445220.6:c.1509C>A ENSP00000489407.2:p.Ser503Arg
ENST00000262795.6:c.2457C>A ENSP00000489147.2:p.Ser819Arg
ENST00000664402.1:c.999C>A ENSP00000499475.1:p.Ser333Arg
ENST00000673971.1:c.*1455C>A ENSP00000501192.1:n.*1455C>A
ENST00000262795.5:c.2853C>A ENSP00000489147.1:p.Ser951Arg
ENST00000414786.6:n.3041C>A
ENST00000445220.5:c.2835C>A ENSP00000489407.1:p.Ser945Arg