Canonical Allele Identifier: CA515264906
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160679T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722251T>C , CM000684.2:g.50722251T>C GRCh38
NC_000022.10:g.51160679T>C , CM000684.1:g.51160679T>C GRCh37
NC_000022.9:g.49507545T>C NCBI36
NG_008607.2:g.52897T>C
NG_070230.1:g.58035T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4019T>C ENSP00000489147.2:p.Leu1340Pro
ENST00000414786.7:n.4603T>C
ENST00000445220.7:c.3071T>C ENSP00000489407.2:p.Leu1024Pro
ENST00000664402.2:c.2561T>C ENSP00000499475.1:p.Leu854Pro
ENST00000673971.2:c.*3017T>C ENSP00000501192.1:n.*3017T>C
ENST00000445220.6:c.3071T>C ENSP00000489407.2:p.Leu1024Pro
ENST00000262795.6:c.4019T>C ENSP00000489147.2:p.Leu1340Pro
ENST00000664402.1:c.2561T>C ENSP00000499475.1:p.Leu854Pro
ENST00000673971.1:c.*3017T>C ENSP00000501192.1:n.*3017T>C
ENST00000262795.5:c.4415T>C ENSP00000489147.1:p.Leu1472Pro
ENST00000414786.6:n.4603T>C
ENST00000445220.5:c.4397T>C ENSP00000489407.1:p.Leu1466Pro