Canonical Allele Identifier: CA515264487
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160549A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722121A>C , CM000684.2:g.50722121A>C GRCh38
NC_000022.10:g.51160549A>C , CM000684.1:g.51160549A>C GRCh37
NC_000022.9:g.49507415A>C NCBI36
NG_008607.2:g.52767A>C
NG_070230.1:g.57905A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3889A>C ENSP00000489147.2:p.Arg1297=
ENST00000414786.7:n.4473A>C
ENST00000445220.7:c.2941A>C ENSP00000489407.2:p.Arg981=
ENST00000664402.2:c.2431A>C ENSP00000499475.1:p.Arg811=
ENST00000673971.2:c.*2887A>C ENSP00000501192.1:n.*2887A>C
ENST00000445220.6:c.2941A>C ENSP00000489407.2:p.Arg981=
ENST00000262795.6:c.3889A>C ENSP00000489147.2:p.Arg1297=
ENST00000664402.1:c.2431A>C ENSP00000499475.1:p.Arg811=
ENST00000673971.1:c.*2887A>C ENSP00000501192.1:n.*2887A>C
ENST00000262795.5:c.4285A>C ENSP00000489147.1:p.Arg1429=
ENST00000414786.6:n.4473A>C
ENST00000445220.5:c.4267A>C ENSP00000489407.1:p.Arg1423=