Canonical Allele Identifier: CA515264476
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160545C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722117C>G , CM000684.2:g.50722117C>G GRCh38
NC_000022.10:g.51160545C>G , CM000684.1:g.51160545C>G GRCh37
NC_000022.9:g.49507411C>G NCBI36
NG_008607.2:g.52763C>G
NG_070230.1:g.57901C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3885C>G ENSP00000489147.2:p.Thr1295=
ENST00000414786.7:n.4469C>G
ENST00000445220.7:c.2937C>G ENSP00000489407.2:p.Thr979=
ENST00000664402.2:c.2427C>G ENSP00000499475.1:p.Thr809=
ENST00000673971.2:c.*2883C>G ENSP00000501192.1:n.*2883C>G
ENST00000445220.6:c.2937C>G ENSP00000489407.2:p.Thr979=
ENST00000262795.6:c.3885C>G ENSP00000489147.2:p.Thr1295=
ENST00000664402.1:c.2427C>G ENSP00000499475.1:p.Thr809=
ENST00000673971.1:c.*2883C>G ENSP00000501192.1:n.*2883C>G
ENST00000262795.5:c.4281C>G ENSP00000489147.1:p.Thr1427=
ENST00000414786.6:n.4469C>G
ENST00000445220.5:c.4263C>G ENSP00000489407.1:p.Thr1421=