Canonical Allele Identifier: CA515263410
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160189C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721761C>T , CM000684.2:g.50721761C>T GRCh38
NC_000022.10:g.51160189C>T , CM000684.1:g.51160189C>T GRCh37
NC_000022.9:g.49507055C>T NCBI36
NG_008607.2:g.52407C>T
NG_070230.1:g.57545C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3529C>T ENSP00000489147.2:p.Pro1177Ser
ENST00000414786.7:n.4113C>T
ENST00000445220.7:c.2581C>T ENSP00000489407.2:p.Pro861Ser
ENST00000664402.2:c.2071C>T ENSP00000499475.1:p.Pro691Ser
ENST00000673971.2:c.*2527C>T ENSP00000501192.1:n.*2527C>T
ENST00000445220.6:c.2581C>T ENSP00000489407.2:p.Pro861Ser
ENST00000262795.6:c.3529C>T ENSP00000489147.2:p.Pro1177Ser
ENST00000664402.1:c.2071C>T ENSP00000499475.1:p.Pro691Ser
ENST00000673971.1:c.*2527C>T ENSP00000501192.1:n.*2527C>T
ENST00000262795.5:c.3925C>T ENSP00000489147.1:p.Pro1309Ser
ENST00000414786.6:n.4113C>T
ENST00000445220.5:c.3907C>T ENSP00000489407.1:p.Pro1303Ser