Canonical Allele Identifier: CA515261410
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159619G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721191G>A , CM000684.2:g.50721191G>A GRCh38
NC_000022.10:g.51159619G>A , CM000684.1:g.51159619G>A GRCh37
NC_000022.9:g.49506485G>A NCBI36
NG_008607.2:g.51837G>A
NG_070230.1:g.56975G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2959G>A ENSP00000489147.2:p.Ala987Thr
ENST00000414786.7:n.3543G>A
ENST00000445220.7:c.2011G>A ENSP00000489407.2:p.Ala671Thr
ENST00000664402.2:c.1501G>A ENSP00000499475.1:p.Ala501Thr
ENST00000673971.2:c.*1957G>A ENSP00000501192.1:n.*1957G>A
ENST00000445220.6:c.2011G>A ENSP00000489407.2:p.Ala671Thr
ENST00000262795.6:c.2959G>A ENSP00000489147.2:p.Ala987Thr
ENST00000664402.1:c.1501G>A ENSP00000499475.1:p.Ala501Thr
ENST00000673971.1:c.*1957G>A ENSP00000501192.1:n.*1957G>A
ENST00000262795.5:c.3355G>A ENSP00000489147.1:p.Ala1119Thr
ENST00000414786.6:n.3543G>A
ENST00000445220.5:c.3337G>A ENSP00000489407.1:p.Ala1113Thr