Canonical Allele Identifier: CA515263766
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160302T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721874T>C , CM000684.2:g.50721874T>C GRCh38
NC_000022.10:g.51160302T>C , CM000684.1:g.51160302T>C GRCh37
NC_000022.9:g.49507168T>C NCBI36
NG_008607.2:g.52520T>C
NG_070230.1:g.57658T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3642T>C ENSP00000489147.2:p.Pro1214=
ENST00000414786.7:n.4226T>C
ENST00000445220.7:c.2694T>C ENSP00000489407.2:p.Pro898=
ENST00000664402.2:c.2184T>C ENSP00000499475.1:p.Pro728=
ENST00000673971.2:c.*2640T>C ENSP00000501192.1:n.*2640T>C
ENST00000445220.6:c.2694T>C ENSP00000489407.2:p.Pro898=
ENST00000262795.6:c.3642T>C ENSP00000489147.2:p.Pro1214=
ENST00000664402.1:c.2184T>C ENSP00000499475.1:p.Pro728=
ENST00000673971.1:c.*2640T>C ENSP00000501192.1:n.*2640T>C
ENST00000262795.5:c.4038T>C ENSP00000489147.1:p.Pro1346=
ENST00000414786.6:n.4226T>C
ENST00000445220.5:c.4020T>C ENSP00000489407.1:p.Pro1340=