Canonical Allele Identifier: CA515262392
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159863C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721435C>A , CM000684.2:g.50721435C>A GRCh38
NC_000022.10:g.51159863C>A , CM000684.1:g.51159863C>A GRCh37
NC_000022.9:g.49506729C>A NCBI36
NG_008607.2:g.52081C>A
NG_070230.1:g.57219C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3203C>A ENSP00000489147.2:p.Thr1068Lys
ENST00000414786.7:n.3787C>A
ENST00000445220.7:c.2255C>A ENSP00000489407.2:p.Thr752Lys
ENST00000664402.2:c.1745C>A ENSP00000499475.1:p.Thr582Lys
ENST00000673971.2:c.*2201C>A ENSP00000501192.1:n.*2201C>A
ENST00000445220.6:c.2255C>A ENSP00000489407.2:p.Thr752Lys
ENST00000262795.6:c.3203C>A ENSP00000489147.2:p.Thr1068Lys
ENST00000664402.1:c.1745C>A ENSP00000499475.1:p.Thr582Lys
ENST00000673971.1:c.*2201C>A ENSP00000501192.1:n.*2201C>A
ENST00000262795.5:c.3599C>A ENSP00000489147.1:p.Thr1200Lys
ENST00000414786.6:n.3787C>A
ENST00000445220.5:c.3581C>A ENSP00000489407.1:p.Thr1194Lys