Canonical Allele Identifier: CA515262469
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159880G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721452G>T , CM000684.2:g.50721452G>T GRCh38
NC_000022.10:g.51159880G>T , CM000684.1:g.51159880G>T GRCh37
NC_000022.9:g.49506746G>T NCBI36
NG_008607.2:g.52098G>T
NG_070230.1:g.57236G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3220G>T ENSP00000489147.2:p.Ala1074Ser
ENST00000414786.7:n.3804G>T
ENST00000445220.7:c.2272G>T ENSP00000489407.2:p.Ala758Ser
ENST00000664402.2:c.1762G>T ENSP00000499475.1:p.Ala588Ser
ENST00000673971.2:c.*2218G>T ENSP00000501192.1:n.*2218G>T
ENST00000445220.6:c.2272G>T ENSP00000489407.2:p.Ala758Ser
ENST00000262795.6:c.3220G>T ENSP00000489147.2:p.Ala1074Ser
ENST00000664402.1:c.1762G>T ENSP00000499475.1:p.Ala588Ser
ENST00000673971.1:c.*2218G>T ENSP00000501192.1:n.*2218G>T
ENST00000262795.5:c.3616G>T ENSP00000489147.1:p.Ala1206Ser
ENST00000414786.6:n.3804G>T
ENST00000445220.5:c.3598G>T ENSP00000489407.1:p.Ala1200Ser