Canonical Allele Identifier: CA515261149
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159526T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721098T>A , CM000684.2:g.50721098T>A GRCh38
NC_000022.10:g.51159526T>A , CM000684.1:g.51159526T>A GRCh37
NC_000022.9:g.49506392T>A NCBI36
NG_008607.2:g.51744T>A
NG_070230.1:g.56882T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2866T>A ENSP00000489147.2:p.Ser956Thr
ENST00000414786.7:n.3450T>A
ENST00000445220.7:c.1918T>A ENSP00000489407.2:p.Ser640Thr
ENST00000664402.2:c.1408T>A ENSP00000499475.1:p.Ser470Thr
ENST00000673971.2:c.*1864T>A ENSP00000501192.1:n.*1864T>A
ENST00000445220.6:c.1918T>A ENSP00000489407.2:p.Ser640Thr
ENST00000262795.6:c.2866T>A ENSP00000489147.2:p.Ser956Thr
ENST00000664402.1:c.1408T>A ENSP00000499475.1:p.Ser470Thr
ENST00000673971.1:c.*1864T>A ENSP00000501192.1:n.*1864T>A
ENST00000262795.5:c.3262T>A ENSP00000489147.1:p.Ser1088Thr
ENST00000414786.6:n.3450T>A
ENST00000445220.5:c.3244T>A ENSP00000489407.1:p.Ser1082Thr