Canonical Allele Identifier: CA515259823
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159057C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720629C>G , CM000684.2:g.50720629C>G GRCh38
NC_000022.10:g.51159057C>G , CM000684.1:g.51159057C>G GRCh37
NC_000022.9:g.49505923C>G NCBI36
NG_008607.2:g.51275C>G
NG_070230.1:g.56413C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2397C>G ENSP00000489147.2:p.Ala799=
ENST00000414786.7:n.2981C>G
ENST00000445220.7:c.1449C>G ENSP00000489407.2:p.Ala483=
ENST00000664402.2:c.939C>G ENSP00000499475.1:p.Ala313=
ENST00000673971.2:c.*1395C>G ENSP00000501192.1:n.*1395C>G
ENST00000445220.6:c.1449C>G ENSP00000489407.2:p.Ala483=
ENST00000262795.6:c.2397C>G ENSP00000489147.2:p.Ala799=
ENST00000664402.1:c.939C>G ENSP00000499475.1:p.Ala313=
ENST00000673971.1:c.*1395C>G ENSP00000501192.1:n.*1395C>G
ENST00000262795.5:c.2793C>G ENSP00000489147.1:p.Ala931=
ENST00000414786.6:n.2981C>G
ENST00000445220.5:c.2775C>G ENSP00000489407.1:p.Ala925=