Canonical Allele Identifier: CA515264563
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160571C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722143C>A , CM000684.2:g.50722143C>A GRCh38
NC_000022.10:g.51160571C>A , CM000684.1:g.51160571C>A GRCh37
NC_000022.9:g.49507437C>A NCBI36
NG_008607.2:g.52789C>A
NG_070230.1:g.57927C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3911C>A ENSP00000489147.2:p.Ser1304Tyr
ENST00000414786.7:n.4495C>A
ENST00000445220.7:c.2963C>A ENSP00000489407.2:p.Ser988Tyr
ENST00000664402.2:c.2453C>A ENSP00000499475.1:p.Ser818Tyr
ENST00000673971.2:c.*2909C>A ENSP00000501192.1:n.*2909C>A
ENST00000445220.6:c.2963C>A ENSP00000489407.2:p.Ser988Tyr
ENST00000262795.6:c.3911C>A ENSP00000489147.2:p.Ser1304Tyr
ENST00000664402.1:c.2453C>A ENSP00000499475.1:p.Ser818Tyr
ENST00000673971.1:c.*2909C>A ENSP00000501192.1:n.*2909C>A
ENST00000262795.5:c.4307C>A ENSP00000489147.1:p.Ser1436Tyr
ENST00000414786.6:n.4495C>A
ENST00000445220.5:c.4289C>A ENSP00000489407.1:p.Ser1430Tyr