Canonical Allele Identifier: CA515260995
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159468G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721040G>C , CM000684.2:g.50721040G>C GRCh38
NC_000022.10:g.51159468G>C , CM000684.1:g.51159468G>C GRCh37
NC_000022.9:g.49506334G>C NCBI36
NG_008607.2:g.51686G>C
NG_070230.1:g.56824G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2808G>C ENSP00000489147.2:p.Leu936=
ENST00000414786.7:n.3392G>C
ENST00000445220.7:c.1860G>C ENSP00000489407.2:p.Leu620=
ENST00000664402.2:c.1350G>C ENSP00000499475.1:p.Leu450=
ENST00000673971.2:c.*1806G>C ENSP00000501192.1:n.*1806G>C
ENST00000445220.6:c.1860G>C ENSP00000489407.2:p.Leu620=
ENST00000262795.6:c.2808G>C ENSP00000489147.2:p.Leu936=
ENST00000664402.1:c.1350G>C ENSP00000499475.1:p.Leu450=
ENST00000673971.1:c.*1806G>C ENSP00000501192.1:n.*1806G>C
ENST00000262795.5:c.3204G>C ENSP00000489147.1:p.Leu1068=
ENST00000414786.6:n.3392G>C
ENST00000445220.5:c.3186G>C ENSP00000489407.1:p.Leu1062=