Canonical Allele Identifier: CA515264367
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160505A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722077A>T , CM000684.2:g.50722077A>T GRCh38
NC_000022.10:g.51160505A>T , CM000684.1:g.51160505A>T GRCh37
NC_000022.9:g.49507371A>T NCBI36
NG_008607.2:g.52723A>T
NG_070230.1:g.57861A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3845A>T ENSP00000489147.2:p.Lys1282Met
ENST00000414786.7:n.4429A>T
ENST00000445220.7:c.2897A>T ENSP00000489407.2:p.Lys966Met
ENST00000664402.2:c.2387A>T ENSP00000499475.1:p.Lys796Met
ENST00000673971.2:c.*2843A>T ENSP00000501192.1:n.*2843A>T
ENST00000445220.6:c.2897A>T ENSP00000489407.2:p.Lys966Met
ENST00000262795.6:c.3845A>T ENSP00000489147.2:p.Lys1282Met
ENST00000664402.1:c.2387A>T ENSP00000499475.1:p.Lys796Met
ENST00000673971.1:c.*2843A>T ENSP00000501192.1:n.*2843A>T
ENST00000262795.5:c.4241A>T ENSP00000489147.1:p.Lys1414Met
ENST00000414786.6:n.4429A>T
ENST00000445220.5:c.4223A>T ENSP00000489407.1:p.Lys1408Met