Canonical Allele Identifier: CA515263573
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160240G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721812G>C , CM000684.2:g.50721812G>C GRCh38
NC_000022.10:g.51160240G>C , CM000684.1:g.51160240G>C GRCh37
NC_000022.9:g.49507106G>C NCBI36
NG_008607.2:g.52458G>C
NG_070230.1:g.57596G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3580G>C ENSP00000489147.2:p.Gly1194Arg
ENST00000414786.7:n.4164G>C
ENST00000445220.7:c.2632G>C ENSP00000489407.2:p.Gly878Arg
ENST00000664402.2:c.2122G>C ENSP00000499475.1:p.Gly708Arg
ENST00000673971.2:c.*2578G>C ENSP00000501192.1:n.*2578G>C
ENST00000445220.6:c.2632G>C ENSP00000489407.2:p.Gly878Arg
ENST00000262795.6:c.3580G>C ENSP00000489147.2:p.Gly1194Arg
ENST00000664402.1:c.2122G>C ENSP00000499475.1:p.Gly708Arg
ENST00000673971.1:c.*2578G>C ENSP00000501192.1:n.*2578G>C
ENST00000262795.5:c.3976G>C ENSP00000489147.1:p.Gly1326Arg
ENST00000414786.6:n.4164G>C
ENST00000445220.5:c.3958G>C ENSP00000489407.1:p.Gly1320Arg