Canonical Allele Identifier: CA515263770
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160303G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721875G>T , CM000684.2:g.50721875G>T GRCh38
NC_000022.10:g.51160303G>T , CM000684.1:g.51160303G>T GRCh37
NC_000022.9:g.49507169G>T NCBI36
NG_008607.2:g.52521G>T
NG_070230.1:g.57659G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3643G>T ENSP00000489147.2:p.Ala1215Ser
ENST00000414786.7:n.4227G>T
ENST00000445220.7:c.2695G>T ENSP00000489407.2:p.Ala899Ser
ENST00000664402.2:c.2185G>T ENSP00000499475.1:p.Ala729Ser
ENST00000673971.2:c.*2641G>T ENSP00000501192.1:n.*2641G>T
ENST00000445220.6:c.2695G>T ENSP00000489407.2:p.Ala899Ser
ENST00000262795.6:c.3643G>T ENSP00000489147.2:p.Ala1215Ser
ENST00000664402.1:c.2185G>T ENSP00000499475.1:p.Ala729Ser
ENST00000673971.1:c.*2641G>T ENSP00000501192.1:n.*2641G>T
ENST00000262795.5:c.4039G>T ENSP00000489147.1:p.Ala1347Ser
ENST00000414786.6:n.4227G>T
ENST00000445220.5:c.4021G>T ENSP00000489407.1:p.Ala1341Ser