Canonical Allele Identifier: CA515264069
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160397T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721969T>G , CM000684.2:g.50721969T>G GRCh38
NC_000022.10:g.51160397T>G , CM000684.1:g.51160397T>G GRCh37
NC_000022.9:g.49507263T>G NCBI36
NG_008607.2:g.52615T>G
NG_070230.1:g.57753T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3737T>G ENSP00000489147.2:p.Val1246Gly
ENST00000414786.7:n.4321T>G
ENST00000445220.7:c.2789T>G ENSP00000489407.2:p.Val930Gly
ENST00000664402.2:c.2279T>G ENSP00000499475.1:p.Val760Gly
ENST00000673971.2:c.*2735T>G ENSP00000501192.1:n.*2735T>G
ENST00000445220.6:c.2789T>G ENSP00000489407.2:p.Val930Gly
ENST00000262795.6:c.3737T>G ENSP00000489147.2:p.Val1246Gly
ENST00000664402.1:c.2279T>G ENSP00000499475.1:p.Val760Gly
ENST00000673971.1:c.*2735T>G ENSP00000501192.1:n.*2735T>G
ENST00000262795.5:c.4133T>G ENSP00000489147.1:p.Val1378Gly
ENST00000414786.6:n.4321T>G
ENST00000445220.5:c.4115T>G ENSP00000489407.1:p.Val1372Gly