Canonical Allele Identifier: CA515261433
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159628G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721200G>A , CM000684.2:g.50721200G>A GRCh38
NC_000022.10:g.51159628G>A , CM000684.1:g.51159628G>A GRCh37
NC_000022.9:g.49506494G>A NCBI36
NG_008607.2:g.51846G>A
NG_070230.1:g.56984G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2968G>A ENSP00000489147.2:p.Ala990Thr
ENST00000414786.7:n.3552G>A
ENST00000445220.7:c.2020G>A ENSP00000489407.2:p.Ala674Thr
ENST00000664402.2:c.1510G>A ENSP00000499475.1:p.Ala504Thr
ENST00000673971.2:c.*1966G>A ENSP00000501192.1:n.*1966G>A
ENST00000445220.6:c.2020G>A ENSP00000489407.2:p.Ala674Thr
ENST00000262795.6:c.2968G>A ENSP00000489147.2:p.Ala990Thr
ENST00000664402.1:c.1510G>A ENSP00000499475.1:p.Ala504Thr
ENST00000673971.1:c.*1966G>A ENSP00000501192.1:n.*1966G>A
ENST00000262795.5:c.3364G>A ENSP00000489147.1:p.Ala1122Thr
ENST00000414786.6:n.3552G>A
ENST00000445220.5:c.3346G>A ENSP00000489407.1:p.Ala1116Thr