Canonical Allele Identifier: CA515264621
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160591G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722163G>C , CM000684.2:g.50722163G>C GRCh38
NC_000022.10:g.51160591G>C , CM000684.1:g.51160591G>C GRCh37
NC_000022.9:g.49507457G>C NCBI36
NG_008607.2:g.52809G>C
NG_070230.1:g.57947G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3931G>C ENSP00000489147.2:p.Ala1311Pro
ENST00000414786.7:n.4515G>C
ENST00000445220.7:c.2983G>C ENSP00000489407.2:p.Ala995Pro
ENST00000664402.2:c.2473G>C ENSP00000499475.1:p.Ala825Pro
ENST00000673971.2:c.*2929G>C ENSP00000501192.1:n.*2929G>C
ENST00000445220.6:c.2983G>C ENSP00000489407.2:p.Ala995Pro
ENST00000262795.6:c.3931G>C ENSP00000489147.2:p.Ala1311Pro
ENST00000664402.1:c.2473G>C ENSP00000499475.1:p.Ala825Pro
ENST00000673971.1:c.*2929G>C ENSP00000501192.1:n.*2929G>C
ENST00000262795.5:c.4327G>C ENSP00000489147.1:p.Ala1443Pro
ENST00000414786.6:n.4515G>C
ENST00000445220.5:c.4309G>C ENSP00000489407.1:p.Ala1437Pro