Canonical Allele Identifier: CA515261828
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159754A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721326A>T , CM000684.2:g.50721326A>T GRCh38
NC_000022.10:g.51159754A>T , CM000684.1:g.51159754A>T GRCh37
NC_000022.9:g.49506620A>T NCBI36
NG_008607.2:g.51972A>T
NG_070230.1:g.57110A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3094A>T ENSP00000489147.2:p.Ser1032Cys
ENST00000414786.7:n.3678A>T
ENST00000445220.7:c.2146A>T ENSP00000489407.2:p.Ser716Cys
ENST00000664402.2:c.1636A>T ENSP00000499475.1:p.Ser546Cys
ENST00000673971.2:c.*2092A>T ENSP00000501192.1:n.*2092A>T
ENST00000445220.6:c.2146A>T ENSP00000489407.2:p.Ser716Cys
ENST00000262795.6:c.3094A>T ENSP00000489147.2:p.Ser1032Cys
ENST00000664402.1:c.1636A>T ENSP00000499475.1:p.Ser546Cys
ENST00000673971.1:c.*2092A>T ENSP00000501192.1:n.*2092A>T
ENST00000262795.5:c.3490A>T ENSP00000489147.1:p.Ser1164Cys
ENST00000414786.6:n.3678A>T
ENST00000445220.5:c.3472A>T ENSP00000489407.1:p.Ser1158Cys