Canonical Allele Identifier: CA515259867
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159071T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720643T>C , CM000684.2:g.50720643T>C GRCh38
NC_000022.10:g.51159071T>C , CM000684.1:g.51159071T>C GRCh37
NC_000022.9:g.49505937T>C NCBI36
NG_008607.2:g.51289T>C
NG_070230.1:g.56427T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2411T>C ENSP00000489147.2:p.Phe804Ser
ENST00000414786.7:n.2995T>C
ENST00000445220.7:c.1463T>C ENSP00000489407.2:p.Phe488Ser
ENST00000664402.2:c.953T>C ENSP00000499475.1:p.Phe318Ser
ENST00000673971.2:c.*1409T>C ENSP00000501192.1:n.*1409T>C
ENST00000445220.6:c.1463T>C ENSP00000489407.2:p.Phe488Ser
ENST00000262795.6:c.2411T>C ENSP00000489147.2:p.Phe804Ser
ENST00000664402.1:c.953T>C ENSP00000499475.1:p.Phe318Ser
ENST00000673971.1:c.*1409T>C ENSP00000501192.1:n.*1409T>C
ENST00000262795.5:c.2807T>C ENSP00000489147.1:p.Phe936Ser
ENST00000414786.6:n.2995T>C
ENST00000445220.5:c.2789T>C ENSP00000489407.1:p.Phe930Ser