Canonical Allele Identifier: CA515262299
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159836A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721408A>T , CM000684.2:g.50721408A>T GRCh38
NC_000022.10:g.51159836A>T , CM000684.1:g.51159836A>T GRCh37
NC_000022.9:g.49506702A>T NCBI36
NG_008607.2:g.52054A>T
NG_070230.1:g.57192A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3176A>T ENSP00000489147.2:p.Lys1059Met
ENST00000414786.7:n.3760A>T
ENST00000445220.7:c.2228A>T ENSP00000489407.2:p.Lys743Met
ENST00000664402.2:c.1718A>T ENSP00000499475.1:p.Lys573Met
ENST00000673971.2:c.*2174A>T ENSP00000501192.1:n.*2174A>T
ENST00000445220.6:c.2228A>T ENSP00000489407.2:p.Lys743Met
ENST00000262795.6:c.3176A>T ENSP00000489147.2:p.Lys1059Met
ENST00000664402.1:c.1718A>T ENSP00000499475.1:p.Lys573Met
ENST00000673971.1:c.*2174A>T ENSP00000501192.1:n.*2174A>T
ENST00000262795.5:c.3572A>T ENSP00000489147.1:p.Lys1191Met
ENST00000414786.6:n.3760A>T
ENST00000445220.5:c.3554A>T ENSP00000489407.1:p.Lys1185Met