Canonical Allele Identifier: CA515263686
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160278G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721850G>C , CM000684.2:g.50721850G>C GRCh38
NC_000022.10:g.51160278G>C , CM000684.1:g.51160278G>C GRCh37
NC_000022.9:g.49507144G>C NCBI36
NG_008607.2:g.52496G>C
NG_070230.1:g.57634G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3618G>C ENSP00000489147.2:p.Gly1206=
ENST00000414786.7:n.4202G>C
ENST00000445220.7:c.2670G>C ENSP00000489407.2:p.Gly890=
ENST00000664402.2:c.2160G>C ENSP00000499475.1:p.Gly720=
ENST00000673971.2:c.*2616G>C ENSP00000501192.1:n.*2616G>C
ENST00000445220.6:c.2670G>C ENSP00000489407.2:p.Gly890=
ENST00000262795.6:c.3618G>C ENSP00000489147.2:p.Gly1206=
ENST00000664402.1:c.2160G>C ENSP00000499475.1:p.Gly720=
ENST00000673971.1:c.*2616G>C ENSP00000501192.1:n.*2616G>C
ENST00000262795.5:c.4014G>C ENSP00000489147.1:p.Gly1338=
ENST00000414786.6:n.4202G>C
ENST00000445220.5:c.3996G>C ENSP00000489407.1:p.Gly1332=