Canonical Allele Identifier: CA515259248
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51158859C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720431C>T , CM000684.2:g.50720431C>T GRCh38
NC_000022.10:g.51158859C>T , CM000684.1:g.51158859C>T GRCh37
NC_000022.9:g.49505725C>T NCBI36
NG_008607.2:g.51077C>T
NG_070230.1:g.56215C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262795.7:c.2199C>T ENSP00000489147.2:p.Gly733=
ENST00000414786.7:n.2783C>T
ENST00000445220.7:c.1251C>T ENSP00000489407.2:p.Gly417=
ENST00000664402.2:c.741C>T ENSP00000499475.1:p.Gly247=
ENST00000673971.2:c.*1197C>T ENSP00000501192.1:n.*1197C>T
ENST00000445220.6:c.1251C>T ENSP00000489407.2:p.Gly417=
ENST00000262795.6:c.2199C>T ENSP00000489147.2:p.Gly733=
ENST00000664402.1:c.741C>T ENSP00000499475.1:p.Gly247=
ENST00000673971.1:c.*1197C>T ENSP00000501192.1:n.*1197C>T
ENST00000262795.5:c.2595C>T ENSP00000489147.1:p.Gly865=
ENST00000414786.6:n.2783C>T
ENST00000445220.5:c.2577C>T ENSP00000489407.1:p.Gly859=