Canonical Allele Identifier: CA515260703
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159361G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720933G>C , CM000684.2:g.50720933G>C GRCh38
NC_000022.10:g.51159361G>C , CM000684.1:g.51159361G>C GRCh37
NC_000022.9:g.49506227G>C NCBI36
NG_008607.2:g.51579G>C
NG_070230.1:g.56717G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2701G>C ENSP00000489147.2:p.Ala901Pro
ENST00000414786.7:n.3285G>C
ENST00000445220.7:c.1753G>C ENSP00000489407.2:p.Ala585Pro
ENST00000664402.2:c.1243G>C ENSP00000499475.1:p.Ala415Pro
ENST00000673971.2:c.*1699G>C ENSP00000501192.1:n.*1699G>C
ENST00000445220.6:c.1753G>C ENSP00000489407.2:p.Ala585Pro
ENST00000262795.6:c.2701G>C ENSP00000489147.2:p.Ala901Pro
ENST00000664402.1:c.1243G>C ENSP00000499475.1:p.Ala415Pro
ENST00000673971.1:c.*1699G>C ENSP00000501192.1:n.*1699G>C
ENST00000262795.5:c.3097G>C ENSP00000489147.1:p.Ala1033Pro
ENST00000414786.6:n.3285G>C
ENST00000445220.5:c.3079G>C ENSP00000489407.1:p.Ala1027Pro