Canonical Allele Identifier: CA515260124
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159157C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720729C>T , CM000684.2:g.50720729C>T GRCh38
NC_000022.10:g.51159157C>T , CM000684.1:g.51159157C>T GRCh37
NC_000022.9:g.49506023C>T NCBI36
NG_008607.2:g.51375C>T
NG_070230.1:g.56513C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2497C>T ENSP00000489147.2:p.Arg833Cys
ENST00000414786.7:n.3081C>T
ENST00000445220.7:c.1549C>T ENSP00000489407.2:p.Arg517Cys
ENST00000664402.2:c.1039C>T ENSP00000499475.1:p.Arg347Cys
ENST00000673971.2:c.*1495C>T ENSP00000501192.1:n.*1495C>T
ENST00000445220.6:c.1549C>T ENSP00000489407.2:p.Arg517Cys
ENST00000262795.6:c.2497C>T ENSP00000489147.2:p.Arg833Cys
ENST00000664402.1:c.1039C>T ENSP00000499475.1:p.Arg347Cys
ENST00000673971.1:c.*1495C>T ENSP00000501192.1:n.*1495C>T
ENST00000262795.5:c.2893C>T ENSP00000489147.1:p.Arg965Cys
ENST00000414786.6:n.3081C>T
ENST00000445220.5:c.2875C>T ENSP00000489407.1:p.Arg959Cys