Canonical Allele Identifier: CA515259158
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51158828A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720400A>T , CM000684.2:g.50720400A>T GRCh38
NC_000022.10:g.51158828A>T , CM000684.1:g.51158828A>T GRCh37
NC_000022.9:g.49505694A>T NCBI36
NG_008607.2:g.51046A>T
NG_070230.1:g.56184A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2168A>T ENSP00000489147.2:p.Lys723Met
ENST00000414786.7:n.2752A>T
ENST00000445220.7:c.1220A>T ENSP00000489407.2:p.Lys407Met
ENST00000664402.2:c.710A>T ENSP00000499475.1:p.Lys237Met
ENST00000673971.2:c.*1166A>T ENSP00000501192.1:n.*1166A>T
ENST00000445220.6:c.1220A>T ENSP00000489407.2:p.Lys407Met
ENST00000262795.6:c.2168A>T ENSP00000489147.2:p.Lys723Met
ENST00000664402.1:c.710A>T ENSP00000499475.1:p.Lys237Met
ENST00000673971.1:c.*1166A>T ENSP00000501192.1:n.*1166A>T
ENST00000262795.5:c.2564A>T ENSP00000489147.1:p.Lys855Met
ENST00000414786.6:n.2752A>T
ENST00000445220.5:c.2546A>T ENSP00000489407.1:p.Lys849Met