Canonical Allele Identifier: CA515264847
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160661T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722233T>C , CM000684.2:g.50722233T>C GRCh38
NC_000022.10:g.51160661T>C , CM000684.1:g.51160661T>C GRCh37
NC_000022.9:g.49507527T>C NCBI36
NG_008607.2:g.52879T>C
NG_070230.1:g.58017T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4001T>C ENSP00000489147.2:p.Phe1334Ser
ENST00000414786.7:n.4585T>C
ENST00000445220.7:c.3053T>C ENSP00000489407.2:p.Phe1018Ser
ENST00000664402.2:c.2543T>C ENSP00000499475.1:p.Phe848Ser
ENST00000673971.2:c.*2999T>C ENSP00000501192.1:n.*2999T>C
ENST00000445220.6:c.3053T>C ENSP00000489407.2:p.Phe1018Ser
ENST00000262795.6:c.4001T>C ENSP00000489147.2:p.Phe1334Ser
ENST00000664402.1:c.2543T>C ENSP00000499475.1:p.Phe848Ser
ENST00000673971.1:c.*2999T>C ENSP00000501192.1:n.*2999T>C
ENST00000262795.5:c.4397T>C ENSP00000489147.1:p.Phe1466Ser
ENST00000414786.6:n.4585T>C
ENST00000445220.5:c.4379T>C ENSP00000489407.1:p.Phe1460Ser